ENST00000389857.11:c.5132G>T
MANE Select
|
ENSP00000374507.6:p.Gly1711Val
|
|
ENST00000331194.8:c.704G>T
|
ENSP00000330332.8:p.Gly235Val
|
|
ENST00000334448.5:n.944G>T
|
|
|
ENST00000389857.10:c.5132G>T
|
ENSP00000374507.6:p.Gly1711Val
|
|
ENST00000556726.5:c.1360G>T
|
|
|
NM_001080414.3:c.5132G>T
|
NP_001073883.2:p.Gly1711Val
|
|
XM_011536796.1:c.5024G>T
|
XP_011535098.1:p.Gly1675Val
|
|
XR_429316.2:n.5407G>T
|
|
|
XM_011536796.2:c.5024G>T
|
XP_011535098.1:p.Gly1675Val
|
|
XM_017021336.1:c.2213G>T
|
XP_016876825.1:p.Gly738Val
|
|
XR_429316.4:n.5405G>T
|
|
|
NM_001080414.4:c.5132G>T
MANE Select
|
NP_001073883.2:p.Gly1711Val
|
|