ENST00000624552.4:c.14914C>T
|
ENSP00000485357.2:p.Pro4972Ser
|
|
ENST00000683500.2:c.14971C>T
MANE Select
|
ENSP00000508292.2:p.Pro4991Ser
|
|
ENST00000623487.1:n.3317C>T
|
|
|
ENST00000624552.3:c.14911C>T
|
ENSP00000485357.1:p.Pro4971Ser
|
|
NM_001291815.1:c.14971C>T
|
NP_001278744.1:p.Pro4991Ser
|
|
XM_011518465.1:c.14848C>T
|
XP_011516767.1:p.Pro4950Ser
|
|
XM_011518466.1:c.14839C>T
|
XP_011516768.1:p.Pro4947Ser
|
|
XM_011518467.1:c.14794C>T
|
XP_011516769.1:p.Pro4932Ser
|
|
NM_001291815.2:c.14971C>T
MANE Select
|
NP_001278744.1:p.Pro4991Ser
|
|
XM_011518465.2:c.14848C>T
|
XP_011516767.1:p.Pro4950Ser
|
|
XM_011518466.2:c.14839C>T
|
XP_011516768.1:p.Pro4947Ser
|
|
XM_011518467.2:c.14794C>T
|
XP_011516769.1:p.Pro4932Ser
|
|
XM_017014585.1:c.11752C>T
|
XP_016870074.1:p.Pro3918Ser
|
|
XM_017014586.1:c.7549C>T
|
XP_016870075.1:p.Pro2517Ser
|
|
XR_001746957.1:n.92+197G>A
|
|
|
XR_001746958.1:n.92+197G>A
|
|
|