ENST00000262304.9:c.3522G>C
MANE Select
|
ENSP00000262304.4:p.Gln1174His
|
|
ENST00000262304.8:c.3522G>C
|
ENSP00000262304.4:p.Gln1174His
|
|
ENST00000415938.7:n.310+695G>C
|
|
|
ENST00000423118.5:c.3522G>C
|
ENSP00000399501.1:p.Gln1174His
|
|
ENST00000468674.5:n.430+695G>C
|
|
|
ENST00000469241.2:n.472G>C
|
|
|
ENST00000483024.1:c.233+171G>C
|
|
|
ENST00000483731.5:n.790+695G>C
|
|
|
ENST00000488185.2:c.473-3287G>C
|
|
|
ENST00000565639.6:n.773+695G>C
|
|
|
ENST00000568591.5:c.2226+695G>C
|
ENSP00000457162.1:n.2226+695G>C
|
|
ENST00000569983.5:n.421+695G>C
|
|
|
NM_000296.3:c.3522G>C
|
NP_000287.3:p.Gln1174His
|
|
NM_001009944.2:c.3522G>C
|
NP_001009944.2:p.Gln1174His
|
|
XM_005255370.2:c.477G>C
|
XP_005255427.1:p.Gln159His
|
|
XM_011522525.1:c.3600G>C
|
XP_011520827.1:p.Gln1200His
|
|
XM_011522526.1:c.3600G>C
|
XP_011520828.1:p.Gln1200His
|
|
XM_011522527.1:c.3600G>C
|
XP_011520829.1:p.Gln1200His
|
|
XM_011522528.1:c.3576G>C
|
XP_011520830.1:p.Gln1192His
|
|
XM_011522529.1:c.3576G>C
|
XP_011520831.1:p.Gln1192His
|
|
XM_011522530.1:c.3546G>C
|
XP_011520832.1:p.Gln1182His
|
|
XM_011522531.1:c.3528G>C
|
XP_011520833.1:p.Gln1176His
|
|
XM_011522532.1:c.3474G>C
|
XP_011520834.1:p.Gln1158His
|
|
XM_011522533.1:c.3393G>C
|
XP_011520835.1:p.Gln1131His
|
|
XM_011522534.1:c.3336G>C
|
XP_011520836.1:p.Gln1112His
|
|
XM_011522535.1:c.1422G>C
|
XP_011520837.1:p.Gln474His
|
|
XM_011522536.1:c.3600G>C
|
XP_011520838.1:p.Gln1200His
|
|
XM_011522537.1:c.600G>C
|
XP_011520839.1:p.Gln200His
|
|
XR_932867.1:n.3615G>C
|
|
|
XR_932868.1:n.3615G>C
|
|
|
XR_932869.1:n.3615G>C
|
|
|
XR_932870.1:n.3615G>C
|
|
|
XM_005255370.3:c.477G>C
|
XP_005255427.1:p.Gln159His
|
|
XM_011522528.3:c.3576G>C
|
XP_011520830.1:p.Gln1192His
|
|
XM_011522529.2:c.3576G>C
|
XP_011520831.1:p.Gln1192His
|
|
XM_011522537.2:c.600G>C
|
XP_011520839.1:p.Gln200His
|
|
XM_024450298.1:c.3642G>C
|
XP_024306066.1:p.Gln1214His
|
|
XM_024450299.1:c.3570G>C
|
XP_024306067.1:p.Gln1190His
|
|
XM_024450300.1:c.3432G>C
|
XP_024306068.1:p.Gln1144His
|
|
XM_024450301.1:c.1518G>C
|
XP_024306069.1:p.Gln506His
|
|
NM_000296.4:c.3522G>C
|
NP_000287.4:p.Gln1174His
|
|
NM_001009944.3:c.3522G>C
MANE Select
|
NP_001009944.3:p.Gln1174His
|
|