ENST00000649046.1:c.12262G>T
MANE Select
|
ENSP00000496870.1:p.Asp4088Tyr
|
|
ENST00000649153.1:c.3162G>T
|
|
|
ENST00000650252.1:c.1290G>T
|
ENSP00000496887.1:p.Leu430Phe
|
|
ENST00000263816.7:c.12262G>T
|
ENSP00000263816.3:p.Asp4088Tyr
|
|
NM_004525.2:c.12262G>T
|
NP_004516.2:p.Asp4088Tyr
|
|
XM_011511183.1:c.12133G>T
|
XP_011509485.1:p.Asp4045Tyr
|
|
XM_011511184.1:c.9973G>T
|
XP_011509486.1:p.Asp3325Tyr
|
|
NM_004525.3:c.12262G>T
MANE Select
|
NP_004516.2:p.Asp4088Tyr
|
|
XM_011511183.3:c.12133G>T
|
XP_011509485.1:p.Asp4045Tyr
|
|
XM_011511184.2:c.9973G>T
|
XP_011509486.1:p.Asp3325Tyr
|
|