ENST00000624552.4:c.14916C>G
|
ENSP00000485357.2:p.Pro4972=
|
|
ENST00000683500.2:c.14973C>G
MANE Select
|
ENSP00000508292.2:p.Pro4991=
|
|
ENST00000623487.1:n.3319C>G
|
|
|
ENST00000624552.3:c.14913C>G
|
ENSP00000485357.1:p.Pro4971=
|
|
NM_001291815.1:c.14973C>G
|
NP_001278744.1:p.Pro4991=
|
|
XM_011518465.1:c.14850C>G
|
XP_011516767.1:p.Pro4950=
|
|
XM_011518466.1:c.14841C>G
|
XP_011516768.1:p.Pro4947=
|
|
XM_011518467.1:c.14796C>G
|
XP_011516769.1:p.Pro4932=
|
|
NM_001291815.2:c.14973C>G
MANE Select
|
NP_001278744.1:p.Pro4991=
|
|
XM_011518465.2:c.14850C>G
|
XP_011516767.1:p.Pro4950=
|
|
XM_011518466.2:c.14841C>G
|
XP_011516768.1:p.Pro4947=
|
|
XM_011518467.2:c.14796C>G
|
XP_011516769.1:p.Pro4932=
|
|
XM_017014585.1:c.11754C>G
|
XP_016870074.1:p.Pro3918=
|
|
XM_017014586.1:c.7551C>G
|
XP_016870075.1:p.Pro2517=
|
|
XR_001746957.1:n.92+195G>C
|
|
|
XR_001746958.1:n.92+195G>C
|
|
|