|
ENST00000262304.9:c.12333C>G
MANE Select
|
ENSP00000262304.4:p.His4111Gln
|
|
|
ENST00000262304.8:c.12333C>G
|
ENSP00000262304.4:p.His4111Gln
|
|
|
ENST00000423118.5:c.12330C>G
|
ENSP00000399501.1:p.His4110Gln
|
|
|
ENST00000472577.1:n.361C>G
|
|
|
|
NM_000296.3:c.12330C>G
|
NP_000287.3:p.His4110Gln
|
|
|
NM_001009944.2:c.12333C>G
|
NP_001009944.2:p.His4111Gln
|
|
|
XM_005255370.2:c.9288C>G
|
XP_005255427.1:p.His3096Gln
|
|
|
XM_011522525.1:c.12411C>G
|
XP_011520827.1:p.His4137Gln
|
|
|
XM_011522526.1:c.12408C>G
|
XP_011520828.1:p.His4136Gln
|
|
|
XM_011522527.1:c.12393C>G
|
XP_011520829.1:p.His4131Gln
|
|
|
XM_011522528.1:c.12387C>G
|
XP_011520830.1:p.His4129Gln
|
|
|
XM_011522529.1:c.12384C>G
|
XP_011520831.1:p.His4128Gln
|
|
|
XM_011522530.1:c.12357C>G
|
XP_011520832.1:p.His4119Gln
|
|
|
XM_011522531.1:c.12339C>G
|
XP_011520833.1:p.His4113Gln
|
|
|
XM_011522532.1:c.12285C>G
|
XP_011520834.1:p.His4095Gln
|
|
|
XM_011522533.1:c.12204C>G
|
XP_011520835.1:p.His4068Gln
|
|
|
XM_011522534.1:c.12147C>G
|
XP_011520836.1:p.His4049Gln
|
|
|
XM_011522535.1:c.10233C>G
|
XP_011520837.1:p.His3411Gln
|
|
|
XM_011522537.1:c.9411C>G
|
XP_011520839.1:p.His3137Gln
|
|
|
XR_932867.1:n.12251C>G
|
|
|
|
XM_005255370.3:c.9288C>G
|
XP_005255427.1:p.His3096Gln
|
|
|
XM_011522528.3:c.12387C>G
|
XP_011520830.1:p.His4129Gln
|
|
|
XM_011522529.2:c.12384C>G
|
XP_011520831.1:p.His4128Gln
|
|
|
XM_011522537.2:c.9411C>G
|
XP_011520839.1:p.His3137Gln
|
|
|
XM_024450298.1:c.12453C>G
|
XP_024306066.1:p.His4151Gln
|
|
|
XM_024450299.1:c.12381C>G
|
XP_024306067.1:p.His4127Gln
|
|
|
XM_024450300.1:c.12243C>G
|
XP_024306068.1:p.His4081Gln
|
|
|
XM_024450301.1:c.10329C>G
|
XP_024306069.1:p.His3443Gln
|
|
|
NM_000296.4:c.12330C>G
|
NP_000287.4:p.His4110Gln
|
|
|
NM_001009944.3:c.12333C>G
MANE Select
|
NP_001009944.3:p.His4111Gln
|
|
