ENST00000318158.11:c.588G>C
MANE Select
|
ENSP00000313432.6:p.Gln196His
|
|
ENST00000318158.10:c.588G>C
|
ENSP00000313432.6:p.Gln196His
|
|
ENST00000377824.8:n.625G>C
|
|
|
ENST00000460882.5:n.615G>C
|
|
|
ENST00000480596.5:n.1289G>C
|
|
|
ENST00000482603.1:n.41G>C
|
|
|
ENST00000491488.5:n.293G>C
|
|
|
ENST00000494290.1:c.159G>C
|
ENSP00000432021.1:p.Gln53His
|
|
ENST00000497693.1:n.2121G>C
|
|
|
ENST00000607784.1:c.588G>C
|
ENSP00000475569.1:p.Gln196His
|
|
NM_012203.1:c.588G>C
|
NP_036335.1:p.Gln196His
|
|
XM_005251631.1:c.267G>C
|
XP_005251688.1:p.Gln89His
|
|
XM_011518073.1:c.186G>C
|
XP_011516375.1:p.Gln62His
|
|
XR_929374.1:n.1033G>C
|
|
|
XM_017015320.2:c.588G>C
|
XP_016870809.1:p.Gln196His
|
|
XM_017015321.2:c.588G>C
|
XP_016870810.1:p.Gln196His
|
|
XM_017015323.2:c.186G>C
|
XP_016870812.1:p.Gln62His
|
|
XM_024447716.1:c.861G>C
|
XP_024303484.1:p.Gln287His
|
|
XM_024447717.1:c.861G>C
|
XP_024303485.1:p.Gln287His
|
|
XR_002956828.1:n.876G>C
|
|
|
XR_002956829.1:n.876G>C
|
|
|
XR_002956830.1:n.647G>C
|
|
|
XR_002956831.1:n.322G>C
|
|
|
XR_002956832.1:n.1007G>C
|
|
|
NM_012203.2:c.588G>C
MANE Select
|
NP_036335.1:p.Gln196His
|
|