ENST00000267845.8:c.1861G>C
MANE Select
|
ENSP00000267845.3:p.Asp621His
|
|
ENST00000267845.7:c.1861G>C
|
ENSP00000267845.3:p.Asp621His
|
|
ENST00000543581.5:c.1762G>C
|
ENSP00000440252.1:p.Asp588His
|
|
ENST00000559816.1:n.1605G>C
|
|
|
NM_001306146.1:c.1762G>C
|
NP_001293075.1:p.Asp588His
|
|
NM_002112.3:c.1861G>C
|
NP_002103.2:p.Asp621His
|
|
XM_011521479.1:c.1624G>C
|
XP_011519781.1:p.Asp542His
|
|
XM_011521480.1:c.1429G>C
|
XP_011519782.1:p.Asp477His
|
|
XM_017022094.1:c.1966G>C
|
XP_016877583.1:p.Asp656His
|
|
XM_017022095.1:c.1867G>C
|
XP_016877584.1:p.Asp623His
|
|
XM_017022096.1:c.1738G>C
|
XP_016877585.1:p.Asp580His
|
|
XM_017022097.1:c.1729G>C
|
XP_016877586.1:p.Asp577His
|
|
XM_017022098.1:c.1534G>C
|
XP_016877587.1:p.Asp512His
|
|
NM_002112.4:c.1861G>C
MANE Select
|
NP_002103.2:p.Asp621His
|
|
NM_001306146.2:c.1762G>C
|
NP_001293075.1:p.Asp588His
|
|