ENST00000624552.4:c.14915C>A
|
ENSP00000485357.2:p.Pro4972His
|
|
ENST00000683500.2:c.14972C>A
MANE Select
|
ENSP00000508292.2:p.Pro4991His
|
|
ENST00000623487.1:n.3318C>A
|
|
|
ENST00000624552.3:c.14912C>A
|
ENSP00000485357.1:p.Pro4971His
|
|
NM_001291815.1:c.14972C>A
|
NP_001278744.1:p.Pro4991His
|
|
XM_011518465.1:c.14849C>A
|
XP_011516767.1:p.Pro4950His
|
|
XM_011518466.1:c.14840C>A
|
XP_011516768.1:p.Pro4947His
|
|
XM_011518467.1:c.14795C>A
|
XP_011516769.1:p.Pro4932His
|
|
NM_001291815.2:c.14972C>A
MANE Select
|
NP_001278744.1:p.Pro4991His
|
|
XM_011518465.2:c.14849C>A
|
XP_011516767.1:p.Pro4950His
|
|
XM_011518466.2:c.14840C>A
|
XP_011516768.1:p.Pro4947His
|
|
XM_011518467.2:c.14795C>A
|
XP_011516769.1:p.Pro4932His
|
|
XM_017014585.1:c.11753C>A
|
XP_016870074.1:p.Pro3918His
|
|
XM_017014586.1:c.7550C>A
|
XP_016870075.1:p.Pro2517His
|
|
XR_001746957.1:n.92+196G>T
|
|
|
XR_001746958.1:n.92+196G>T
|
|
|