ENST00000324071.10:c.1220C>T
MANE Select
|
ENSP00000324648.2:p.Ala407Val
|
|
ENST00000598834.2:c.1177-232C>T
|
|
|
ENST00000324071.8:c.1220C>T
|
ENSP00000324648.2:p.Ala407Val
|
|
ENST00000593831.1:c.512C>T
|
ENSP00000470582.1:p.Ala171Val
|
|
ENST00000597612.1:n.647+256C>T
|
|
|
NM_000767.4:c.1220C>T
|
NP_000758.1:p.Ala407Val
|
|
XM_005258569.3:c.1152+256C>T
|
XP_005258626.1:n.1152+256C>T
|
|
XM_006723050.2:c.1220C>T
|
XP_006723113.1:p.Ala407Val
|
|
XM_011526546.1:c.1153-75C>T
|
XP_011524848.1:n.1153-75C>T
|
|
XM_011526547.1:c.1153-232C>T
|
XP_011524849.1:n.1153-232C>T
|
|
XM_011526548.1:c.740C>T
|
XP_011524850.1:p.Ala247Val
|
|
XM_011526549.1:c.629C>T
|
XP_011524851.1:p.Ala210Val
|
|
XM_011526550.1:c.620C>T
|
XP_011524852.1:p.Ala207Val
|
|
NM_000767.5:c.1220C>T
MANE Select
|
NP_000758.1:p.Ala407Val
|
|