ENST00000541682.7:c.268G>T
MANE Select
|
ENSP00000446205.2:p.Ala90Ser
|
|
ENST00000317814.8:c.253G>T
|
ENSP00000314774.4:p.Ala85Ser
|
|
ENST00000541682.6:c.268G>T
|
ENSP00000446205.2:p.Ala90Ser
|
|
ENST00000577735.1:c.244G>T
|
ENSP00000462491.1:p.Ala82Ser
|
|
NM_001165967.1:c.268G>T
|
NP_001159439.1:p.Ala90Ser
|
|
NM_032580.3:c.253G>T
|
NP_115969.2:p.Ala85Ser
|
|
XM_011524038.1:c.373G>T
|
XP_011522340.1:p.Ala125Ser
|
|
XM_011524039.1:c.364G>T
|
XP_011522341.1:p.Ala122Ser
|
|
XM_011524040.1:c.364G>T
|
XP_011522342.1:p.Ala122Ser
|
|
XM_011524041.1:c.355G>T
|
XP_011522343.1:p.Ala119Ser
|
|
XM_011524042.1:c.226G>T
|
XP_011522344.1:p.Ala76Ser
|
|
XR_934203.1:n.69+2182C>A
|
|
|
XM_017025232.1:c.373G>T
|
XP_016880721.1:p.Ala125Ser
|
|
XM_024451007.1:c.373G>T
|
XP_024306775.1:p.Ala125Ser
|
|
NM_001165967.2:c.268G>T
MANE Select
|
NP_001159439.1:p.Ala90Ser
|
|
NM_032580.4:c.253G>T
|
NP_115969.2:p.Ala85Ser
|
|