ENST00000326003.7:c.735G>A
MANE Select
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ENSP00000314151.1:p.Lys245=
|
|
ENST00000326003.6:c.735G>A
|
ENSP00000314151.1:p.Lys245=
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|
ENST00000360617.7:c.1177G>A
|
ENSP00000353829.2:n.1177G>A
|
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ENST00000422986.6:c.*391G>A
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ENSP00000393628.2:n.*391G>A
|
|
ENST00000595392.5:c.*236G>A
|
ENSP00000468912.1:n.*236G>A
|
|
ENST00000595952.5:c.606G>A
|
ENSP00000471155.1:p.Lys202=
|
|
ENST00000596333.1:n.913G>A
|
|
|
ENST00000598145.1:c.737G>A
|
|
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ENST00000601349.5:n.2014G>A
|
|
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ENST00000601812.1:n.1167G>A
|
|
|
ENST00000617027.4:c.612G>A
|
ENSP00000483513.1:p.Lys204=
|
|
NM_001030047.1:c.*460G>A
|
NP_001025218.1:n.*460G>A
|
|
NM_001030048.1:c.606G>A
|
NP_001025219.1:p.Lys202=
|
|
NM_001648.2:c.735G>A
MANE Select
|
NP_001639.1:p.Lys245=
|
|
XM_011526923.1:c.753G>A
|
XP_011525225.1:p.Lys251=
|
|
XR_935817.1:n.1324+822G>A
|
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