ENST00000367698.4:c.1357A>G
MANE Select
|
ENSP00000356671.3:p.Ile453Val
|
|
ENST00000367698.3:c.1357A>G
|
ENSP00000356671.3:p.Ile453Val
|
|
ENST00000617423.4:c.742A>G
|
ENSP00000478688.1:p.Ile248Val
|
|
NM_000488.3:c.1357A>G , LRG_577t1:c.1357A>G
|
NP_000479.1:p.Ile453Val
|
|
XM_005245198.2:c.1213A>G
|
XP_005245255.1:p.Ile405Val
|
|
NM_001365052.1:c.1213A>G
|
NP_001351981.1:p.Ile405Val
|
|
NM_000488.4:c.1357A>G
MANE Select
|
NP_000479.1:p.Ile453Val
|
|
NM_001365052.2:c.1213A>G
|
NP_001351981.1:p.Ile405Val
|
|
NM_001386302.1:c.1480A>G
|
NP_001373231.1:p.Ile494Val
|
|
NM_001386303.1:c.1438A>G
|
NP_001373232.1:p.Ile480Val
|
|
NM_001386304.1:c.1336A>G
|
NP_001373233.1:p.Ile446Val
|
|
NM_001386305.1:c.1300A>G
|
NP_001373234.1:p.Ile434Val
|
|
NM_001386306.1:c.1141A>G
|
NP_001373235.1:p.Ile381Val
|
|