ENST00000624552.4:c.14867G>A
|
ENSP00000485357.2:p.Cys4956Tyr
|
|
ENST00000683500.2:c.14924G>A
MANE Select
|
ENSP00000508292.2:p.Cys4975Tyr
|
|
ENST00000623487.1:n.3270G>A
|
|
|
ENST00000624552.3:c.14864G>A
|
ENSP00000485357.1:p.Cys4955Tyr
|
|
NM_001291815.1:c.14924G>A
|
NP_001278744.1:p.Cys4975Tyr
|
|
XM_011518465.1:c.14801G>A
|
XP_011516767.1:p.Cys4934Tyr
|
|
XM_011518466.1:c.14792G>A
|
XP_011516768.1:p.Cys4931Tyr
|
|
XM_011518467.1:c.14747G>A
|
XP_011516769.1:p.Cys4916Tyr
|
|
NM_001291815.2:c.14924G>A
MANE Select
|
NP_001278744.1:p.Cys4975Tyr
|
|
XM_011518465.2:c.14801G>A
|
XP_011516767.1:p.Cys4934Tyr
|
|
XM_011518466.2:c.14792G>A
|
XP_011516768.1:p.Cys4931Tyr
|
|
XM_011518467.2:c.14747G>A
|
XP_011516769.1:p.Cys4916Tyr
|
|
XM_017014585.1:c.11705G>A
|
XP_016870074.1:p.Cys3902Tyr
|
|
XM_017014586.1:c.7502G>A
|
XP_016870075.1:p.Cys2501Tyr
|
|
XR_001746957.1:n.92+244C>T
|
|
|
XR_001746958.1:n.92+244C>T
|
|
|