ENST00000298229.7:c.1118T>C
MANE Select
|
ENSP00000298229.2:p.Val373Ala
|
|
ENST00000298229.6:c.1118T>C
|
ENSP00000298229.2:p.Val373Ala
|
|
ENST00000538751.5:c.392T>C
|
ENSP00000444619.1:p.Val131Ala
|
|
ENST00000540329.5:c.302T>C
|
ENSP00000440018.1:p.Val101Ala
|
|
ENST00000541756.5:c.920T>C
|
ENSP00000446360.2:p.Val307Ala
|
|
NM_001567.3:c.1118T>C
|
NP_001558.3:p.Val373Ala
|
|
XM_005273978.3:c.1184T>C
|
XP_005274035.1:p.Val395Ala
|
|
XM_005273979.3:c.1184T>C
|
XP_005274036.1:p.Val395Ala
|
|
XM_011544999.1:c.1118T>C
|
XP_011543301.1:p.Val373Ala
|
|
XM_011545000.1:c.1184T>C
|
XP_011543302.1:p.Val395Ala
|
|
XM_005273979.4:c.1184T>C
|
XP_005274036.1:p.Val395Ala
|
|
XM_011544999.2:c.1118T>C
|
XP_011543301.1:p.Val373Ala
|
|
XM_024448501.1:c.1184T>C
|
XP_024304269.1:p.Val395Ala
|
|
XM_024448502.1:c.1184T>C
|
XP_024304270.1:p.Val395Ala
|
|
XM_024448503.1:c.1154T>C
|
XP_024304271.1:p.Val385Ala
|
|
XM_024448504.1:c.1118T>C
|
XP_024304272.1:p.Val373Ala
|
|
XM_024448505.1:c.1184T>C
|
XP_024304273.1:p.Val395Ala
|
|
NM_001567.4:c.1118T>C
MANE Select
|
NP_001558.3:p.Val373Ala
|
|