ENST00000247933.9:c.1081G=
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ENSP00000247933.4:p.Ala361=
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ENST00000514224.2:c.1081G=
MANE Select
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ENSP00000425081.2:p.Ala361=
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ENST00000652070.1:n.1137G=
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|
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ENST00000247933.8:c.1081G=
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ENSP00000247933.4:p.Ala361=
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ENST00000514224.1:c.685G=
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ENSP00000425081.1:p.Ala229=
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ENST00000514698.5:n.1188G=
|
|
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NM_000203.4:c.1081G=
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NP_000194.2:p.Ala361=
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NR_110313.1:n.1169G=
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|
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XM_006713882.2:c.685G=
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XP_006713945.1:p.Ala229=
|
|
XM_011513459.1:c.1147G=
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XP_011511761.1:p.Ala383=
|
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XM_011513460.1:c.940G=
|
XP_011511762.1:p.Ala314=
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XM_011513461.1:c.874G=
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XP_011511763.1:p.Ala292=
|
|
XM_011513462.1:c.793G=
|
XP_011511764.1:p.Ala265=
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XM_011513463.1:c.793G=
|
XP_011511765.1:p.Ala265=
|
|
XR_924947.1:n.1150G=
|
|
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NM_000203.5:c.1081G=
MANE Select
|
NP_000194.2:p.Ala361=
|
|
NM_001363576.1:c.685G=
|
NP_001350505.1:p.Ala229=
|
|
XM_011513461.2:c.874G=
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XP_011511763.1:p.Ala292=
|
|
XM_017008163.1:c.121G=
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XP_016863652.1:p.Ala41=
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