ENST00000318158.11:c.577G>T
MANE Select
|
ENSP00000313432.6:p.Ala193Ser
|
|
ENST00000318158.10:c.577G>T
|
ENSP00000313432.6:p.Ala193Ser
|
|
ENST00000377824.8:n.614G>T
|
|
|
ENST00000460882.5:n.604G>T
|
|
|
ENST00000480596.5:n.1278G>T
|
|
|
ENST00000482603.1:n.30G>T
|
|
|
ENST00000491488.5:n.282G>T
|
|
|
ENST00000494290.1:c.148G>T
|
ENSP00000432021.1:p.Ala50Ser
|
|
ENST00000497693.1:n.2110G>T
|
|
|
ENST00000607784.1:c.577G>T
|
ENSP00000475569.1:p.Ala193Ser
|
|
NM_012203.1:c.577G>T
|
NP_036335.1:p.Ala193Ser
|
|
XM_005251631.1:c.256G>T
|
XP_005251688.1:p.Ala86Ser
|
|
XM_011518073.1:c.175G>T
|
XP_011516375.1:p.Ala59Ser
|
|
XR_929374.1:n.1022G>T
|
|
|
XM_017015320.2:c.577G>T
|
XP_016870809.1:p.Ala193Ser
|
|
XM_017015321.2:c.577G>T
|
XP_016870810.1:p.Ala193Ser
|
|
XM_017015323.2:c.175G>T
|
XP_016870812.1:p.Ala59Ser
|
|
XM_024447716.1:c.850G>T
|
XP_024303484.1:p.Ala284Ser
|
|
XM_024447717.1:c.850G>T
|
XP_024303485.1:p.Ala284Ser
|
|
XR_002956828.1:n.865G>T
|
|
|
XR_002956829.1:n.865G>T
|
|
|
XR_002956830.1:n.636G>T
|
|
|
XR_002956831.1:n.311G>T
|
|
|
XR_002956832.1:n.996G>T
|
|
|
NM_012203.2:c.577G>T
MANE Select
|
NP_036335.1:p.Ala193Ser
|
|