ENST00000324071.10:c.1248C>T
MANE Select
|
ENSP00000324648.2:p.Ala416=
|
|
ENST00000598834.2:c.1177-204C>T
|
|
|
ENST00000324071.8:c.1248C>T
|
ENSP00000324648.2:p.Ala416=
|
|
ENST00000593831.1:c.540C>T
|
ENSP00000470582.1:p.Ala180=
|
|
ENST00000597612.1:n.647+284C>T
|
|
|
NM_000767.4:c.1248C>T
|
NP_000758.1:p.Ala416=
|
|
XM_005258569.3:c.1152+284C>T
|
XP_005258626.1:n.1152+284C>T
|
|
XM_006723050.2:c.1248C>T
|
XP_006723113.1:p.Ala416=
|
|
XM_011526546.1:c.1153-47C>T
|
XP_011524848.1:n.1153-47C>T
|
|
XM_011526547.1:c.1153-204C>T
|
XP_011524849.1:n.1153-204C>T
|
|
XM_011526548.1:c.768C>T
|
XP_011524850.1:p.Ala256=
|
|
XM_011526549.1:c.657C>T
|
XP_011524851.1:p.Ala219=
|
|
XM_011526550.1:c.648C>T
|
XP_011524852.1:p.Ala216=
|
|
NM_000767.5:c.1248C>T
MANE Select
|
NP_000758.1:p.Ala416=
|
|