ENST00000267845.8:c.1834G>T
MANE Select
|
ENSP00000267845.3:p.Val612Phe
|
|
ENST00000267845.7:c.1834G>T
|
ENSP00000267845.3:p.Val612Phe
|
|
ENST00000543581.5:c.1735G>T
|
ENSP00000440252.1:p.Val579Phe
|
|
ENST00000559816.1:n.1578G>T
|
|
|
NM_001306146.1:c.1735G>T
|
NP_001293075.1:p.Val579Phe
|
|
NM_002112.3:c.1834G>T
|
NP_002103.2:p.Val612Phe
|
|
XM_011521479.1:c.1597G>T
|
XP_011519781.1:p.Val533Phe
|
|
XM_011521480.1:c.1402G>T
|
XP_011519782.1:p.Val468Phe
|
|
XM_017022094.1:c.1939G>T
|
XP_016877583.1:p.Val647Phe
|
|
XM_017022095.1:c.1840G>T
|
XP_016877584.1:p.Val614Phe
|
|
XM_017022096.1:c.1711G>T
|
XP_016877585.1:p.Val571Phe
|
|
XM_017022097.1:c.1702G>T
|
XP_016877586.1:p.Val568Phe
|
|
XM_017022098.1:c.1507G>T
|
XP_016877587.1:p.Val503Phe
|
|
NM_002112.4:c.1834G>T
MANE Select
|
NP_002103.2:p.Val612Phe
|
|
NM_001306146.2:c.1735G>T
|
NP_001293075.1:p.Val579Phe
|
|