ENST00000624552.4:c.14969T>C
|
ENSP00000485357.2:p.Val4990Ala
|
|
ENST00000683500.2:c.15026T>C
MANE Select
|
ENSP00000508292.2:p.Val5009Ala
|
|
ENST00000623487.1:n.3372T>C
|
|
|
ENST00000624552.3:c.14966T>C
|
ENSP00000485357.1:p.Val4989Ala
|
|
NM_001291815.1:c.15026T>C
|
NP_001278744.1:p.Val5009Ala
|
|
XM_011518465.1:c.14903T>C
|
XP_011516767.1:p.Val4968Ala
|
|
XM_011518466.1:c.14894T>C
|
XP_011516768.1:p.Val4965Ala
|
|
XM_011518467.1:c.14849T>C
|
XP_011516769.1:p.Val4950Ala
|
|
NM_001291815.2:c.15026T>C
MANE Select
|
NP_001278744.1:p.Val5009Ala
|
|
XM_011518465.2:c.14903T>C
|
XP_011516767.1:p.Val4968Ala
|
|
XM_011518466.2:c.14894T>C
|
XP_011516768.1:p.Val4965Ala
|
|
XM_011518467.2:c.14849T>C
|
XP_011516769.1:p.Val4950Ala
|
|
XM_017014585.1:c.11807T>C
|
XP_016870074.1:p.Val3936Ala
|
|
XM_017014586.1:c.7604T>C
|
XP_016870075.1:p.Val2535Ala
|
|
XR_001746957.1:n.92+142A>G
|
|
|
XR_001746958.1:n.92+142A>G
|
|
|