ENST00000318158.11:c.534G>T
MANE Select
|
ENSP00000313432.6:p.Gln178His
|
|
ENST00000318158.10:c.534G>T
|
ENSP00000313432.6:p.Gln178His
|
|
ENST00000377824.8:n.571G>T
|
|
|
ENST00000460882.5:n.561G>T
|
|
|
ENST00000480596.5:n.1235G>T
|
|
|
ENST00000491488.5:n.239G>T
|
|
|
ENST00000494290.1:c.105G>T
|
ENSP00000432021.1:p.Gln35His
|
|
ENST00000497693.1:n.2067G>T
|
|
|
ENST00000607784.1:c.534G>T
|
ENSP00000475569.1:p.Gln178His
|
|
NM_012203.1:c.534G>T
|
NP_036335.1:p.Gln178His
|
|
XM_005251631.1:c.213G>T
|
XP_005251688.1:p.Gln71His
|
|
XM_011518073.1:c.132G>T
|
XP_011516375.1:p.Gln44His
|
|
XR_929374.1:n.979G>T
|
|
|
XM_017015320.2:c.534G>T
|
XP_016870809.1:p.Gln178His
|
|
XM_017015321.2:c.534G>T
|
XP_016870810.1:p.Gln178His
|
|
XM_017015323.2:c.132G>T
|
XP_016870812.1:p.Gln44His
|
|
XM_024447716.1:c.807G>T
|
XP_024303484.1:p.Gln269His
|
|
XM_024447717.1:c.807G>T
|
XP_024303485.1:p.Gln269His
|
|
XR_002956828.1:n.822G>T
|
|
|
XR_002956829.1:n.822G>T
|
|
|
XR_002956830.1:n.593G>T
|
|
|
XR_002956831.1:n.268G>T
|
|
|
XR_002956832.1:n.953G>T
|
|
|
NM_012203.2:c.534G>T
MANE Select
|
NP_036335.1:p.Gln178His
|
|