ENST00000624552.4:c.14962T>G
|
ENSP00000485357.2:p.Ser4988Ala
|
|
ENST00000683500.2:c.15019T>G
MANE Select
|
ENSP00000508292.2:p.Ser5007Ala
|
|
ENST00000623487.1:n.3365T>G
|
|
|
ENST00000624552.3:c.14959T>G
|
ENSP00000485357.1:p.Ser4987Ala
|
|
NM_001291815.1:c.15019T>G
|
NP_001278744.1:p.Ser5007Ala
|
|
XM_011518465.1:c.14896T>G
|
XP_011516767.1:p.Ser4966Ala
|
|
XM_011518466.1:c.14887T>G
|
XP_011516768.1:p.Ser4963Ala
|
|
XM_011518467.1:c.14842T>G
|
XP_011516769.1:p.Ser4948Ala
|
|
NM_001291815.2:c.15019T>G
MANE Select
|
NP_001278744.1:p.Ser5007Ala
|
|
XM_011518465.2:c.14896T>G
|
XP_011516767.1:p.Ser4966Ala
|
|
XM_011518466.2:c.14887T>G
|
XP_011516768.1:p.Ser4963Ala
|
|
XM_011518467.2:c.14842T>G
|
XP_011516769.1:p.Ser4948Ala
|
|
XM_017014585.1:c.11800T>G
|
XP_016870074.1:p.Ser3934Ala
|
|
XM_017014586.1:c.7597T>G
|
XP_016870075.1:p.Ser2533Ala
|
|
XR_001746957.1:n.92+149A>C
|
|
|
XR_001746958.1:n.92+149A>C
|
|
|