ENST00000262304.9:c.2182C>G
MANE Select
|
ENSP00000262304.4:p.His728Asp
|
|
ENST00000262304.8:c.2182C>G
|
ENSP00000262304.4:p.His728Asp
|
|
ENST00000423118.5:c.2182C>G
|
ENSP00000399501.1:p.His728Asp
|
|
ENST00000488185.2:c.472+2648C>G
|
|
|
ENST00000568591.5:c.1113C>G
|
ENSP00000457162.1:n.1113C>G
|
|
NM_000296.3:c.2182C>G
|
NP_000287.3:p.His728Asp
|
|
NM_001009944.2:c.2182C>G
|
NP_001009944.2:p.His728Asp
|
|
XM_011522525.1:c.2236C>G
|
XP_011520827.1:p.His746Asp
|
|
XM_011522526.1:c.2236C>G
|
XP_011520828.1:p.His746Asp
|
|
XM_011522527.1:c.2236C>G
|
XP_011520829.1:p.His746Asp
|
|
XM_011522528.1:c.2236C>G
|
XP_011520830.1:p.His746Asp
|
|
XM_011522529.1:c.2236C>G
|
XP_011520831.1:p.His746Asp
|
|
XM_011522530.1:c.2182C>G
|
XP_011520832.1:p.His728Asp
|
|
XM_011522531.1:c.2164C>G
|
XP_011520833.1:p.His722Asp
|
|
XM_011522532.1:c.2110C>G
|
XP_011520834.1:p.His704Asp
|
|
XM_011522533.1:c.2029C>G
|
XP_011520835.1:p.His677Asp
|
|
XM_011522534.1:c.1972C>G
|
XP_011520836.1:p.His658Asp
|
|
XM_011522535.1:c.58C>G
|
XP_011520837.1:p.His20Asp
|
|
XM_011522536.1:c.2236C>G
|
XP_011520838.1:p.His746Asp
|
|
XR_932867.1:n.2251C>G
|
|
|
XR_932868.1:n.2251C>G
|
|
|
XR_932869.1:n.2251C>G
|
|
|
XR_932870.1:n.2251C>G
|
|
|
XM_011522528.3:c.2236C>G
|
XP_011520830.1:p.His746Asp
|
|
XM_011522529.2:c.2236C>G
|
XP_011520831.1:p.His746Asp
|
|
XM_024450298.1:c.2182C>G
|
XP_024306066.1:p.His728Asp
|
|
XM_024450299.1:c.2110C>G
|
XP_024306067.1:p.His704Asp
|
|
XM_024450300.1:c.1972C>G
|
XP_024306068.1:p.His658Asp
|
|
XM_024450301.1:c.58C>G
|
XP_024306069.1:p.His20Asp
|
|
NM_000296.4:c.2182C>G
|
NP_000287.4:p.His728Asp
|
|
NM_001009944.3:c.2182C>G
MANE Select
|
NP_001009944.3:p.His728Asp
|
|