ENST00000318158.11:c.753G>T
MANE Select
|
ENSP00000313432.6:p.Gln251His
|
|
ENST00000318158.10:c.753G>T
|
ENSP00000313432.6:p.Gln251His
|
|
ENST00000460882.5:n.780G>T
|
|
|
ENST00000480596.5:n.1454G>T
|
|
|
ENST00000482603.1:n.206G>T
|
|
|
ENST00000491488.5:n.458G>T
|
|
|
ENST00000494290.1:c.*51+875G>T
|
ENSP00000432021.1:n.*51+875G>T
|
|
ENST00000497693.1:n.4321G>T
|
|
|
ENST00000607784.1:c.753G>T
|
ENSP00000475569.1:p.Gln251His
|
|
NM_012203.1:c.753G>T
|
NP_036335.1:p.Gln251His
|
|
XM_005251631.1:c.432G>T
|
XP_005251688.1:p.Gln144His
|
|
XM_011518073.1:c.351G>T
|
XP_011516375.1:p.Gln117His
|
|
XM_017015320.2:c.753G>T
|
XP_016870809.1:p.Gln251His
|
|
XM_017015321.2:c.753G>T
|
XP_016870810.1:p.Gln251His
|
|
XM_017015323.2:c.351G>T
|
XP_016870812.1:p.Gln117His
|
|
XM_024447716.1:c.1026G>T
|
XP_024303484.1:p.Gln342His
|
|
XM_024447717.1:c.1026G>T
|
XP_024303485.1:p.Gln342His
|
|
XR_002956828.1:n.1041G>T
|
|
|
XR_002956829.1:n.1041G>T
|
|
|
XR_002956830.1:n.2173G>T
|
|
|
XR_002956831.1:n.1848G>T
|
|
|
XR_002956832.1:n.1172G>T
|
|
|
NM_012203.2:c.753G>T
MANE Select
|
NP_036335.1:p.Gln251His
|
|