|
ENST00000460011.6:c.-90G>T
|
ENSP00000507070.1:n.-90G>T
|
|
|
ENST00000494498.2:c.109G>T
|
ENSP00000507847.1:p.Ala37Ser
|
|
|
ENST00000397746.8:c.1375G>T
MANE Select
|
ENSP00000380854.3:p.Ala459Ser
|
|
|
ENST00000291670.9:c.1375G>T
|
ENSP00000291670.5:p.Ala459Ser
|
|
|
ENST00000397743.1:c.1331G>T
|
ENSP00000380851.1:p.Gly444Val
|
|
|
ENST00000397746.7:c.1375G>T
|
ENSP00000380854.3:p.Ala459Ser
|
|
|
ENST00000397748.5:c.1375G>T
|
ENSP00000380856.1:p.Ala459Ser
|
|
|
ENST00000460011.5:n.704G>T
|
|
|
|
ENST00000488577.1:n.401G>T
|
|
|
|
ENST00000494498.1:n.676G>T
|
|
|
|
ENST00000498355.6:n.1444G>T
|
|
|
|
NM_006657.2:c.1375G>T
|
NP_006648.1:p.Ala459Ser
|
|
|
NM_206965.1:c.1375G>T
|
NP_996848.1:p.Ala459Ser
|
|
|
XM_006723961.2:c.1624G>T
|
XP_006724024.2:p.Ala542Ser
|
|
|
XM_006723962.2:c.1624G>T
|
XP_006724025.2:p.Ala542Ser
|
|
|
XM_011529434.1:c.1624G>T
|
XP_011527736.1:p.Ala542Ser
|
|
|
XM_011529435.1:c.1495G>T
|
XP_011527737.1:p.Ala499Ser
|
|
|
XM_011529436.1:c.1624G>T
|
XP_011527738.1:p.Ala542Ser
|
|
|
XM_011529437.1:c.1624G>T
|
XP_011527739.1:p.Ala542Ser
|
|
|
XM_011529438.1:c.1495G>T
|
XP_011527740.1:p.Ala499Ser
|
|
|
XM_011529439.1:c.1111G>T
|
XP_011527741.1:p.Ala371Ser
|
|
|
XR_937433.1:n.1807G>T
|
|
|
|
NM_001320412.1:c.1375G>T
|
NP_001307341.1:p.Ala459Ser
|
|
|
XM_006723961.4:c.1624G>T
|
XP_006724024.2:p.Ala542Ser
|
|
|
XM_006723962.4:c.1624G>T
|
XP_006724025.2:p.Ala542Ser
|
|
|
XM_011529434.3:c.1624G>T
|
XP_011527736.1:p.Ala542Ser
|
|
|
XM_011529435.3:c.1495G>T
|
XP_011527737.1:p.Ala499Ser
|
|
|
XM_011529436.3:c.1624G>T
|
XP_011527738.1:p.Ala542Ser
|
|
|
XM_011529437.3:c.1624G>T
|
XP_011527739.1:p.Ala542Ser
|
|
|
XM_011529439.2:c.1111G>T
|
XP_011527741.1:p.Ala371Ser
|
|
|
XR_937433.3:n.1841G>T
|
|
|
|
NM_206965.2:c.1375G>T
MANE Select
|
NP_996848.1:p.Ala459Ser
|
|
|
NM_001320412.2:c.1375G>T
|
NP_001307341.1:p.Ala459Ser
|
|
|
NM_006657.3:c.1375G>T
|
NP_006648.1:p.Ala459Ser
|
|
