ENST00000318158.11:c.507T>C
MANE Select
|
ENSP00000313432.6:p.Ala169=
|
|
ENST00000318158.10:c.507T>C
|
ENSP00000313432.6:p.Ala169=
|
|
ENST00000377824.8:n.544T>C
|
|
|
ENST00000460882.5:n.534T>C
|
|
|
ENST00000480596.5:n.1208T>C
|
|
|
ENST00000491488.5:n.212T>C
|
|
|
ENST00000494290.1:c.78T>C
|
ENSP00000432021.1:p.Ala26=
|
|
ENST00000497693.1:n.2040T>C
|
|
|
ENST00000607784.1:c.507T>C
|
ENSP00000475569.1:p.Ala169=
|
|
NM_012203.1:c.507T>C
|
NP_036335.1:p.Ala169=
|
|
XM_005251631.1:c.186T>C
|
XP_005251688.1:p.Ala62=
|
|
XM_011518073.1:c.105T>C
|
XP_011516375.1:p.Ala35=
|
|
XR_929374.1:n.952T>C
|
|
|
XM_017015320.2:c.507T>C
|
XP_016870809.1:p.Ala169=
|
|
XM_017015321.2:c.507T>C
|
XP_016870810.1:p.Ala169=
|
|
XM_017015323.2:c.105T>C
|
XP_016870812.1:p.Ala35=
|
|
XM_024447716.1:c.780T>C
|
XP_024303484.1:p.Ala260=
|
|
XM_024447717.1:c.780T>C
|
XP_024303485.1:p.Ala260=
|
|
XR_002956828.1:n.795T>C
|
|
|
XR_002956829.1:n.795T>C
|
|
|
XR_002956830.1:n.566T>C
|
|
|
XR_002956831.1:n.241T>C
|
|
|
XR_002956832.1:n.926T>C
|
|
|
NM_012203.2:c.507T>C
MANE Select
|
NP_036335.1:p.Ala169=
|
|