ENST00000391944.8:c.1834C>G
|
ENSP00000375808.4:p.His612Asp
|
|
ENST00000682414.1:c.1834C>G
|
ENSP00000507019.1:p.His612Asp
|
|
ENST00000682508.1:n.1863C>G
|
|
|
ENST00000684218.1:c.*1092C>G
|
ENSP00000507804.1:n.*1092C>G
|
|
ENST00000684264.1:n.1390C>G
|
|
|
ENST00000684407.1:c.1711C>G
|
ENSP00000507775.1:p.His571Asp
|
|
ENST00000684458.1:c.*320C>G
|
ENSP00000508260.1:n.*320C>G
|
|
ENST00000684468.1:n.1546C>G
|
|
|
ENST00000391945.10:c.1834C>G
MANE Select
|
ENSP00000375809.4:p.His612Asp
|
|
ENST00000646507.1:n.1931C>G
|
|
|
ENST00000391941.6:c.1762C>G
|
ENSP00000375805.2:p.His588Asp
|
|
ENST00000391942.6:n.1005C>G
|
|
|
ENST00000391944.7:c.1600C>G
|
ENSP00000375808.3:p.His534Asp
|
|
ENST00000391945.8:c.1834C>G
|
ENSP00000375809.3:p.His612Asp
|
|
ENST00000588652.5:n.1922C>G
|
|
|
NM_000400.3:c.1834C>G , LRG_461t1:c.1834C>G
|
NP_000391.1:p.His612Asp
|
|
XM_011526611.1:c.1756C>G
|
XP_011524913.1:p.His586Asp
|
|
XM_011526611.2:c.1756C>G
|
XP_011524913.1:p.His586Asp
|
|
XM_017026467.1:c.1711C>G
|
XP_016881956.1:p.His571Asp
|
|
XR_001753633.2:n.1881C>G
|
|
|
XR_001753634.2:n.1817C>G
|
|
|
NM_000400.4:c.1834C>G
MANE Select
|
NP_000391.1:p.His612Asp
|
|