ENST00000367698.4:c.1358T>G
MANE Select
|
ENSP00000356671.3:p.Ile453Ser
|
|
ENST00000367698.3:c.1358T>G
|
ENSP00000356671.3:p.Ile453Ser
|
|
ENST00000617423.4:c.743T>G
|
ENSP00000478688.1:p.Ile248Ser
|
|
NM_000488.3:c.1358T>G , LRG_577t1:c.1358T>G
|
NP_000479.1:p.Ile453Ser
|
|
XM_005245198.2:c.1214T>G
|
XP_005245255.1:p.Ile405Ser
|
|
NM_001365052.1:c.1214T>G
|
NP_001351981.1:p.Ile405Ser
|
|
NM_000488.4:c.1358T>G
MANE Select
|
NP_000479.1:p.Ile453Ser
|
|
NM_001365052.2:c.1214T>G
|
NP_001351981.1:p.Ile405Ser
|
|
NM_001386302.1:c.1481T>G
|
NP_001373231.1:p.Ile494Ser
|
|
NM_001386303.1:c.1439T>G
|
NP_001373232.1:p.Ile480Ser
|
|
NM_001386304.1:c.1337T>G
|
NP_001373233.1:p.Ile446Ser
|
|
NM_001386305.1:c.1301T>G
|
NP_001373234.1:p.Ile434Ser
|
|
NM_001386306.1:c.1142T>G
|
NP_001373235.1:p.Ile381Ser
|
|