ENST00000624552.4:c.14908C>G
|
ENSP00000485357.2:p.Pro4970Ala
|
|
ENST00000683500.2:c.14965C>G
MANE Select
|
ENSP00000508292.2:p.Pro4989Ala
|
|
ENST00000623487.1:n.3311C>G
|
|
|
ENST00000624552.3:c.14905C>G
|
ENSP00000485357.1:p.Pro4969Ala
|
|
NM_001291815.1:c.14965C>G
|
NP_001278744.1:p.Pro4989Ala
|
|
XM_011518465.1:c.14842C>G
|
XP_011516767.1:p.Pro4948Ala
|
|
XM_011518466.1:c.14833C>G
|
XP_011516768.1:p.Pro4945Ala
|
|
XM_011518467.1:c.14788C>G
|
XP_011516769.1:p.Pro4930Ala
|
|
NM_001291815.2:c.14965C>G
MANE Select
|
NP_001278744.1:p.Pro4989Ala
|
|
XM_011518465.2:c.14842C>G
|
XP_011516767.1:p.Pro4948Ala
|
|
XM_011518466.2:c.14833C>G
|
XP_011516768.1:p.Pro4945Ala
|
|
XM_011518467.2:c.14788C>G
|
XP_011516769.1:p.Pro4930Ala
|
|
XM_017014585.1:c.11746C>G
|
XP_016870074.1:p.Pro3916Ala
|
|
XM_017014586.1:c.7543C>G
|
XP_016870075.1:p.Pro2515Ala
|
|
XR_001746957.1:n.92+203G>C
|
|
|
XR_001746958.1:n.92+203G>C
|
|
|