|
ENST00000704781.1:c.748+1162A>G
|
ENSP00000516029.1:n.748+1162A>G
|
|
|
ENST00000704782.1:c.748+1162A>G
|
ENSP00000516031.1:n.748+1162A>G
|
|
|
ENST00000409571.6:c.748+1162A>G
|
ENSP00000386416.1:n.748+1162A>G
|
|
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ENST00000417749.6:c.748+1162A>G
|
ENSP00000411271.2:n.748+1162A>G
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|
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ENST00000437746.2:c.748+1162A>G
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ENSP00000412211.2:n.748+1162A>G
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|
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ENST00000688050.1:c.748+1162A>G
|
ENSP00000509497.1:n.748+1162A>G
|
|
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ENST00000265459.11:c.748+1162A>G
MANE Select
|
ENSP00000265459.5:n.748+1162A>G
|
|
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ENST00000265459.10:c.748+1162A>G
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ENSP00000265459.5:n.748+1162A>G
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ENST00000377551.5:c.748+1162A>G
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ENSP00000366774.1:n.748+1162A>G
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ENST00000377559.7:c.748+1162A>G
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ENSP00000366782.3:n.748+1162A>G
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ENST00000409571.5:c.748+1162A>G
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ENSP00000386416.1:n.748+1162A>G
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|
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ENST00000417749.5:c.30+1162A>G
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|
|
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ENST00000437746.1:c.146+1162A>G
|
|
|
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ENST00000442300.5:c.61+1162A>G
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ENSP00000388971.1:n.61+1162A>G
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|
|
ENST00000466324.1:n.992+1162A>G
|
|
|
|
NM_015080.3:c.748+1162A>G
|
NP_055895.1:n.748+1162A>G
|
|
|
NM_138732.2:c.748+1162A>G
|
NP_620060.1:n.748+1162A>G
|
|
|
XM_005274400.3:c.748+1162A>G
|
XP_005274457.1:n.748+1162A>G
|
|
|
XM_005274401.3:c.748+1162A>G
|
XP_005274458.1:n.748+1162A>G
|
|
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XM_005274402.3:c.748+1162A>G
|
XP_005274459.1:n.748+1162A>G
|
|
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XM_006718742.2:c.748+1162A>G
|
XP_006718805.2:n.748+1162A>G
|
|
|
XM_006718745.2:c.748+1162A>G
|
XP_006718808.2:n.748+1162A>G
|
|
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XM_011545365.1:c.748+1162A>G
|
XP_011543667.1:n.748+1162A>G
|
|
|
XM_011545366.1:c.748+1162A>G
|
XP_011543668.1:n.748+1162A>G
|
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XM_011545367.1:c.748+1162A>G
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XP_011543669.1:n.748+1162A>G
|
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XM_011545368.1:c.748+1162A>G
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XP_011543670.1:n.748+1162A>G
|
|
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XM_011545369.1:c.748+1162A>G
|
XP_011543671.1:n.748+1162A>G
|
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XM_011545370.1:c.748+1162A>G
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XP_011543672.1:n.748+1162A>G
|
|
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XM_011545371.1:c.748+1162A>G
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XP_011543673.1:n.748+1162A>G
|
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XM_011545372.1:c.748+1162A>G
|
XP_011543674.1:n.748+1162A>G
|
|
|
XM_011545373.1:c.748+1162A>G
|
XP_011543675.1:n.748+1162A>G
|
|
|
XM_011545374.1:c.748+1162A>G
|
XP_011543676.1:n.748+1162A>G
|
|
|
XM_011545375.1:c.748+1162A>G
|
XP_011543677.1:n.748+1162A>G
|
|
|
XM_011545376.1:c.748+1162A>G
|
XP_011543678.1:n.748+1162A>G
|
|
|
XM_011545377.1:c.748+1162A>G
|
XP_011543679.1:n.748+1162A>G
|
|
|
XM_011545378.1:c.748+1162A>G
|
XP_011543680.1:n.748+1162A>G
|
|
|
XM_011545379.1:c.43+1162A>G
|
XP_011543681.1:n.43+1162A>G
|
|
|
XM_011545380.1:c.37+1162A>G
|
XP_011543682.1:n.37+1162A>G
|
|
|
XM_011545381.1:c.43+1162A>G
|
XP_011543683.1:n.43+1162A>G
|
|
|
XM_011545382.1:c.43+1162A>G
|
XP_011543684.1:n.43+1162A>G
|
|
|
XM_011545383.1:c.7+1162A>G
|
XP_011543685.1:n.7+1162A>G
|
|
|
XM_011545387.1:c.748+1162A>G
|
XP_011543689.1:n.748+1162A>G
|
|
|
XR_950109.1:n.763+1162A>G
|
|
|
|
XR_950110.1:n.763+1162A>G
|
|
|
|
XR_950111.1:n.763+1162A>G
|
|
|
|
XM_017018563.1:c.748+1162A>G
|
XP_016874052.1:n.748+1162A>G
|
|
|
XM_017018564.1:c.748+1162A>G
|
XP_016874053.1:n.748+1162A>G
|
|
|
XM_017018565.1:c.748+1162A>G
|
XP_016874054.1:n.748+1162A>G
|
|
|
XM_017018566.1:c.748+1162A>G
|
XP_016874055.1:n.748+1162A>G
|
|
|
XM_017018567.1:c.748+1162A>G
|
XP_016874056.1:n.748+1162A>G
|
|
|
XM_017018568.1:c.748+1162A>G
|
XP_016874057.1:n.748+1162A>G
|
|
|
XM_017018569.1:c.748+1162A>G
|
XP_016874058.1:n.748+1162A>G
|
|
|
XM_017018570.1:c.748+1162A>G
|
XP_016874059.1:n.748+1162A>G
|
|
|
XM_017018571.1:c.748+1162A>G
|
XP_016874060.1:n.748+1162A>G
|
|
|
XM_017018572.1:c.43+1162A>G
|
XP_016874061.1:n.43+1162A>G
|
|
|
XM_017018573.1:c.748+1162A>G
|
XP_016874062.1:n.748+1162A>G
|
|
|
XM_017018574.1:c.43+1162A>G
|
XP_016874063.1:n.43+1162A>G
|
|
|
XM_017018575.1:c.43+1162A>G
|
XP_016874064.1:n.43+1162A>G
|
|
|
XM_017018578.1:c.748+1162A>G
|
XP_016874067.1:n.748+1162A>G
|
|
|
XM_024448770.1:c.748+1162A>G
|
XP_024304538.1:n.748+1162A>G
|
|
|
XM_024448771.1:c.748+1162A>G
|
XP_024304539.1:n.748+1162A>G
|
|
|
XM_024448772.1:c.748+1162A>G
|
XP_024304540.1:n.748+1162A>G
|
|
|
XM_024448773.1:c.748+1162A>G
|
XP_024304541.1:n.748+1162A>G
|
|
|
XM_024448775.1:c.748+1162A>G
|
XP_024304543.1:n.748+1162A>G
|
|
|
XM_024448776.1:c.748+1162A>G
|
XP_024304544.1:n.748+1162A>G
|
|
|
XR_001748042.1:n.763+1162A>G
|
|
|
|
XR_001748043.2:n.763+1162A>G
|
|
|
|
XR_001748044.1:n.763+1162A>G
|
|
|
|
NM_001376262.1:c.748+1162A>G
|
NP_001363191.1:n.748+1162A>G
|
|
|
NM_001376263.1:c.748+1162A>G
|
NP_001363192.1:n.748+1162A>G
|
|
|
NM_001376265.1:c.748+1162A>G
|
NP_001363194.1:n.748+1162A>G
|
|
|
NM_001376266.1:c.748+1162A>G
|
NP_001363195.1:n.748+1162A>G
|
|
|
NM_001376267.1:c.748+1162A>G
|
NP_001363196.1:n.748+1162A>G
|
|
|
NM_015080.4:c.748+1162A>G
MANE Select
|
NP_055895.1:n.748+1162A>G
|
|
|
NM_138732.3:c.748+1162A>G
|
NP_620060.1:n.748+1162A>G
|
|
