ENST00000261769.10:c.2623A>G
MANE Select
|
ENSP00000261769.4:p.Met875Val
|
|
ENST00000261769.9:c.2623A>G
|
ENSP00000261769.4:p.Met875Val
|
|
ENST00000422392.6:c.2440A>G
|
ENSP00000414946.2:p.Met814Val
|
|
ENST00000562118.1:n.841A>G
|
|
|
ENST00000562836.5:n.2694A>G
|
|
|
ENST00000566510.5:c.*1289A>G
|
ENSP00000458139.1:n.*1289A>G
|
|
ENST00000566612.5:c.*863A>G
|
ENSP00000454782.1:n.*863A>G
|
|
ENST00000611625.4:c.2686A>G
|
ENSP00000481063.1:p.Met896Val
|
|
ENST00000612417.4:c.1854-718A>G
|
ENSP00000478360.1:n.1854-718A>G
|
|
ENST00000621016.4:c.1866-730A>G
|
ENSP00000480664.1:n.1866-730A>G
|
|
NM_004360.3:c.2623A>G , LRG_301t1:c.2623A>G
|
NP_004351.1:p.Met875Val
|
|
XM_011523488.1:c.1888A>G
|
XP_011521790.1:p.Met630Val
|
|
XM_011523489.1:c.1888A>G
|
XP_011521791.1:p.Met630Val
|
|
NM_001317184.1:c.2440A>G
|
NP_001304113.1:p.Met814Val
|
|
NM_001317185.1:c.1075A>G
|
NP_001304114.1:p.Met359Val
|
|
NM_001317186.1:c.658A>G
|
NP_001304115.1:p.Met220Val
|
|
NM_004360.4:c.2623A>G
|
NP_004351.1:p.Met875Val
|
|
NM_004360.5:c.2623A>G
MANE Select
|
NP_004351.1:p.Met875Val
|
|
NM_001317184.2:c.2440A>G
|
NP_001304113.1:p.Met814Val
|
|
NM_001317185.2:c.1075A>G
|
NP_001304114.1:p.Met359Val
|
|
NM_001317186.2:c.658A>G
|
NP_001304115.1:p.Met220Val
|
|