ENST00000374479.4:c.1112C>T
MANE Select
|
ENSP00000363603.3:p.Ala371Val
|
|
ENST00000374479.3:c.1112C>T
|
ENSP00000363603.3:p.Ala371Val
|
|
NM_000147.4:c.1112C>T
|
NP_000138.2:p.Ala371Val
|
|
XM_005245821.1:c.737C>T
|
XP_005245878.1:p.Ala246Val
|
|
XM_011541167.1:c.479C>T
|
XP_011539469.1:p.Ala160Val
|
|
XM_005245821.3:c.737C>T
|
XP_005245878.1:p.Ala246Val
|
|
XM_011541167.3:c.479C>T
|
XP_011539469.1:p.Ala160Val
|
|
XM_017000905.2:c.809C>T
|
XP_016856394.1:p.Ala270Val
|
|
NM_000147.5:c.1112C>T
MANE Select
|
NP_000138.2:p.Ala371Val
|
|
NR_174379.1:n.1290C>T
|
|
|
NR_174380.1:n.1339C>T
|
|
|
NR_174381.1:n.1178C>T
|
|
|
NR_174382.1:n.1575C>T
|
|
|