ENST00000318158.11:c.531C>T
MANE Select
|
ENSP00000313432.6:p.Val177=
|
|
ENST00000318158.10:c.531C>T
|
ENSP00000313432.6:p.Val177=
|
|
ENST00000377824.8:n.568C>T
|
|
|
ENST00000460882.5:n.558C>T
|
|
|
ENST00000480596.5:n.1232C>T
|
|
|
ENST00000491488.5:n.236C>T
|
|
|
ENST00000494290.1:c.102C>T
|
ENSP00000432021.1:p.Val34=
|
|
ENST00000497693.1:n.2064C>T
|
|
|
ENST00000607784.1:c.531C>T
|
ENSP00000475569.1:p.Val177=
|
|
NM_012203.1:c.531C>T
|
NP_036335.1:p.Val177=
|
|
XM_005251631.1:c.210C>T
|
XP_005251688.1:p.Val70=
|
|
XM_011518073.1:c.129C>T
|
XP_011516375.1:p.Val43=
|
|
XR_929374.1:n.976C>T
|
|
|
XM_017015320.2:c.531C>T
|
XP_016870809.1:p.Val177=
|
|
XM_017015321.2:c.531C>T
|
XP_016870810.1:p.Val177=
|
|
XM_017015323.2:c.129C>T
|
XP_016870812.1:p.Val43=
|
|
XM_024447716.1:c.804C>T
|
XP_024303484.1:p.Val268=
|
|
XM_024447717.1:c.804C>T
|
XP_024303485.1:p.Val268=
|
|
XR_002956828.1:n.819C>T
|
|
|
XR_002956829.1:n.819C>T
|
|
|
XR_002956830.1:n.590C>T
|
|
|
XR_002956831.1:n.265C>T
|
|
|
XR_002956832.1:n.950C>T
|
|
|
NM_012203.2:c.531C>T
MANE Select
|
NP_036335.1:p.Val177=
|
|