ENST00000367698.4:c.1358T>A
MANE Select
|
ENSP00000356671.3:p.Ile453Asn
|
|
ENST00000367698.3:c.1358T>A
|
ENSP00000356671.3:p.Ile453Asn
|
|
ENST00000617423.4:c.743T>A
|
ENSP00000478688.1:p.Ile248Asn
|
|
NM_000488.3:c.1358T>A , LRG_577t1:c.1358T>A
|
NP_000479.1:p.Ile453Asn
|
|
XM_005245198.2:c.1214T>A
|
XP_005245255.1:p.Ile405Asn
|
|
NM_001365052.1:c.1214T>A
|
NP_001351981.1:p.Ile405Asn
|
|
NM_000488.4:c.1358T>A
MANE Select
|
NP_000479.1:p.Ile453Asn
|
|
NM_001365052.2:c.1214T>A
|
NP_001351981.1:p.Ile405Asn
|
|
NM_001386302.1:c.1481T>A
|
NP_001373231.1:p.Ile494Asn
|
|
NM_001386303.1:c.1439T>A
|
NP_001373232.1:p.Ile480Asn
|
|
NM_001386304.1:c.1337T>A
|
NP_001373233.1:p.Ile446Asn
|
|
NM_001386305.1:c.1301T>A
|
NP_001373234.1:p.Ile434Asn
|
|
NM_001386306.1:c.1142T>A
|
NP_001373235.1:p.Ile381Asn
|
|