ENST00000324071.10:c.1152G>A
MANE Select
|
ENSP00000324648.2:p.Lys384=
|
|
ENST00000598834.2:c.1176G>A
|
|
|
ENST00000324071.8:c.1152G>A
|
ENSP00000324648.2:p.Lys384=
|
|
ENST00000593831.1:c.444G>A
|
ENSP00000470582.1:p.Lys148=
|
|
ENST00000597612.1:n.647G>A
|
|
|
NM_000767.4:c.1152G>A
|
NP_000758.1:p.Lys384=
|
|
XM_005258569.3:c.1152G>A
|
XP_005258626.1:p.Lys384=
|
|
XM_006723050.2:c.1152G>A
|
XP_006723113.1:p.Lys384=
|
|
XM_011526546.1:c.1152G>A
|
XP_011524848.1:p.Lys384=
|
|
XM_011526547.1:c.1152G>A
|
XP_011524849.1:p.Lys384=
|
|
XM_011526548.1:c.672G>A
|
XP_011524850.1:p.Lys224=
|
|
XM_011526549.1:c.561G>A
|
XP_011524851.1:p.Lys187=
|
|
XM_011526550.1:c.552G>A
|
XP_011524852.1:p.Lys184=
|
|
NM_000767.5:c.1152G>A
MANE Select
|
NP_000758.1:p.Lys384=
|
|