|
NM_021939.4:c.1363A>G
MANE Select
|
NP_068758.3:p.Ile455Val
|
|
ENST00000321562.9:c.1363A>G
MANE Select
|
ENSP00000317232.4:p.Ile455Val
|
|
NM_021939.3:c.1363A>G , LRG_12t1:c.1363A>G
|
NP_068758.3:p.Ile455Val
|
|
ENST00000321562.8:c.1363A>G
|
ENSP00000317232.4:p.Ile455Val
|
|
ENST00000455106.1:c.774A>G
|
|
|
ENST00000464180.1:n.611A>G
|
|
|
ENST00000489591.5:c.*1147A>G
|
ENSP00000466352.1:n.*1147A>G
|
|
ENST00000490938.5:n.566A>G
|
|
|
ENST00000706683.1:c.1027A>G
|
ENSP00000516497.1:p.Ile343Val
|
|
XM_011525099.1:c.1420A>G
|
XP_011523401.1:p.Ile474Val
|
|
XM_011525099.3:c.1420A>G
|
XP_011523401.1:p.Ile474Val
|
|
XM_011525100.1:c.1147A>G
|
XP_011523402.1:p.Ile383Val
|
|
XM_011525100.2:c.1147A>G
|
XP_011523402.1:p.Ile383Val
|