ENST00000391944.8:c.1858A>G
|
ENSP00000375808.4:p.Met620Val
|
|
ENST00000682414.1:c.1858A>G
|
ENSP00000507019.1:p.Met620Val
|
|
ENST00000682508.1:n.1887A>G
|
|
|
ENST00000684218.1:c.*1116A>G
|
ENSP00000507804.1:n.*1116A>G
|
|
ENST00000684264.1:n.1414A>G
|
|
|
ENST00000684407.1:c.1735A>G
|
ENSP00000507775.1:p.Met579Val
|
|
ENST00000684458.1:c.*344A>G
|
ENSP00000508260.1:n.*344A>G
|
|
ENST00000684468.1:n.1570A>G
|
|
|
ENST00000391945.10:c.1858A>G
MANE Select
|
ENSP00000375809.4:p.Met620Val
|
|
ENST00000646507.1:n.1955A>G
|
|
|
ENST00000391941.6:c.1786A>G
|
ENSP00000375805.2:p.Met596Val
|
|
ENST00000391942.6:n.1029A>G
|
|
|
ENST00000391944.7:c.1624A>G
|
ENSP00000375808.3:p.Met542Val
|
|
ENST00000391945.8:c.1858A>G
|
ENSP00000375809.3:p.Met620Val
|
|
ENST00000588652.5:n.1946A>G
|
|
|
NM_000400.3:c.1858A>G , LRG_461t1:c.1858A>G
|
NP_000391.1:p.Met620Val
|
|
XM_011526611.1:c.1780A>G
|
XP_011524913.1:p.Met594Val
|
|
XM_011526611.2:c.1780A>G
|
XP_011524913.1:p.Met594Val
|
|
XM_017026467.1:c.1735A>G
|
XP_016881956.1:p.Met579Val
|
|
XR_001753633.2:n.1905A>G
|
|
|
XR_001753634.2:n.1841A>G
|
|
|
NM_000400.4:c.1858A>G
MANE Select
|
NP_000391.1:p.Met620Val
|
|