ENST00000342741.6:c.426A>T
MANE Select
|
ENSP00000339933.4:p.Ala142=
|
|
ENST00000434082.3:c.234A>T
|
ENSP00000398037.3:p.Ala78=
|
|
ENST00000342741.4:c.426A>T
|
ENSP00000339933.4:p.Ala142=
|
|
ENST00000392414.7:c.333A>T
|
ENSP00000376214.3:p.Ala111=
|
|
ENST00000434082.2:c.331A>T
|
ENSP00000398037.2:n.331A>T
|
|
NM_000298.5:c.426A>T
|
NP_000289.1:p.Ala142=
|
|
NM_181871.3:c.333A>T
|
NP_870986.1:p.Ala111=
|
|
XM_005245266.3:c.585A>T
|
XP_005245323.1:p.Ala195=
|
|
XM_006711386.2:c.234A>T
|
XP_006711449.1:p.Ala78=
|
|
XM_011509639.1:c.585A>T
|
XP_011507941.1:p.Ala195=
|
|
XM_011509640.1:c.234A>T
|
XP_011507942.1:p.Ala78=
|
|
NM_000298.6:c.426A>T
MANE Select
|
NP_000289.1:p.Ala142=
|
|
XM_006711386.4:c.234A>T
|
XP_006711449.1:p.Ala78=
|
|
XM_011509640.3:c.234A>T
|
XP_011507942.1:p.Ala78=
|
|
XM_017001493.1:c.426A>T
|
XP_016856982.1:p.Ala142=
|
|
NM_181871.4:c.333A>T
|
NP_870986.1:p.Ala111=
|
|