ENST00000324071.10:c.1159G>C
MANE Select
|
ENSP00000324648.2:p.Glu387Gln
|
|
ENST00000598834.2:c.1176+195G>C
|
|
|
ENST00000324071.8:c.1159G>C
|
ENSP00000324648.2:p.Glu387Gln
|
|
ENST00000593831.1:c.451G>C
|
ENSP00000470582.1:p.Glu151Gln
|
|
ENST00000597612.1:n.647+195G>C
|
|
|
NM_000767.4:c.1159G>C
|
NP_000758.1:p.Glu387Gln
|
|
XM_005258569.3:c.1152+195G>C
|
XP_005258626.1:n.1152+195G>C
|
|
XM_006723050.2:c.1159G>C
|
XP_006723113.1:p.Glu387Gln
|
|
XM_011526546.1:c.1153-136G>C
|
XP_011524848.1:n.1153-136G>C
|
|
XM_011526547.1:c.1152+195G>C
|
XP_011524849.1:n.1152+195G>C
|
|
XM_011526548.1:c.679G>C
|
XP_011524850.1:p.Glu227Gln
|
|
XM_011526549.1:c.568G>C
|
XP_011524851.1:p.Glu190Gln
|
|
XM_011526550.1:c.559G>C
|
XP_011524852.1:p.Glu187Gln
|
|
NM_000767.5:c.1159G>C
MANE Select
|
NP_000758.1:p.Glu387Gln
|
|