ENST00000324071.10:c.1153G>T
MANE Select
|
ENSP00000324648.2:p.Asp385Tyr
|
|
ENST00000598834.2:c.1176+189G>T
|
|
|
ENST00000324071.8:c.1153G>T
|
ENSP00000324648.2:p.Asp385Tyr
|
|
ENST00000593831.1:c.445G>T
|
ENSP00000470582.1:p.Asp149Tyr
|
|
ENST00000597612.1:n.647+189G>T
|
|
|
NM_000767.4:c.1153G>T
|
NP_000758.1:p.Asp385Tyr
|
|
XM_005258569.3:c.1152+189G>T
|
XP_005258626.1:n.1152+189G>T
|
|
XM_006723050.2:c.1153G>T
|
XP_006723113.1:p.Asp385Tyr
|
|
XM_011526546.1:c.1153-142G>T
|
XP_011524848.1:n.1153-142G>T
|
|
XM_011526547.1:c.1152+189G>T
|
XP_011524849.1:n.1152+189G>T
|
|
XM_011526548.1:c.673G>T
|
XP_011524850.1:p.Asp225Tyr
|
|
XM_011526549.1:c.562G>T
|
XP_011524851.1:p.Asp188Tyr
|
|
XM_011526550.1:c.553G>T
|
XP_011524852.1:p.Asp185Tyr
|
|
NM_000767.5:c.1153G>T
MANE Select
|
NP_000758.1:p.Asp385Tyr
|
|