ENST00000477226.6:n.847T>G
|
|
|
ENST00000683013.1:n.761T>G
|
|
|
ENST00000373960.4:c.1373T>G
MANE Select
|
ENSP00000363071.3:p.Val458Gly
|
|
ENST00000373960.3:c.1373T>G
|
ENSP00000363071.3:p.Val458Gly
|
|
ENST00000483395.1:n.228T>G
|
|
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NM_001927.3:c.1373T>G , LRG_380t1:c.1373T>G
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NP_001918.3:p.Val458Gly
|
|
NM_001927.4:c.1373T>G
MANE Select
|
NP_001918.3:p.Val458Gly
|
|
NM_001382708.1:c.1370T>G
|
NP_001369637.1:p.Val457Gly
|
|
NM_001382709.1:c.941T>G
|
NP_001369638.1:p.Val314Gly
|
|
NM_001382710.1:c.1304T>G
|
NP_001369639.1:p.Val435Gly
|
|
NM_001382711.1:c.1352T>G
|
NP_001369640.1:p.Val451Gly
|
|
NM_001382712.1:c.1371+205T>G
|
NP_001369641.1:n.1371+205T>G
|
|
NM_001382713.1:c.1103T>G
|
NP_001369642.1:p.Val368Gly
|
|