ENST00000624552.4:c.14884T>G
|
ENSP00000485357.2:p.Ser4962Ala
|
|
ENST00000683500.2:c.14941T>G
MANE Select
|
ENSP00000508292.2:p.Ser4981Ala
|
|
ENST00000623487.1:n.3287T>G
|
|
|
ENST00000624552.3:c.14881T>G
|
ENSP00000485357.1:p.Ser4961Ala
|
|
NM_001291815.1:c.14941T>G
|
NP_001278744.1:p.Ser4981Ala
|
|
XM_011518465.1:c.14818T>G
|
XP_011516767.1:p.Ser4940Ala
|
|
XM_011518466.1:c.14809T>G
|
XP_011516768.1:p.Ser4937Ala
|
|
XM_011518467.1:c.14764T>G
|
XP_011516769.1:p.Ser4922Ala
|
|
NM_001291815.2:c.14941T>G
MANE Select
|
NP_001278744.1:p.Ser4981Ala
|
|
XM_011518465.2:c.14818T>G
|
XP_011516767.1:p.Ser4940Ala
|
|
XM_011518466.2:c.14809T>G
|
XP_011516768.1:p.Ser4937Ala
|
|
XM_011518467.2:c.14764T>G
|
XP_011516769.1:p.Ser4922Ala
|
|
XM_017014585.1:c.11722T>G
|
XP_016870074.1:p.Ser3908Ala
|
|
XM_017014586.1:c.7519T>G
|
XP_016870075.1:p.Ser2507Ala
|
|
XR_001746957.1:n.92+227A>C
|
|
|
XR_001746958.1:n.92+227A>C
|
|
|