ENST00000367698.4:c.1320C>T
MANE Select
|
ENSP00000356671.3:p.Phe440=
|
|
ENST00000367698.3:c.1320C>T
|
ENSP00000356671.3:p.Phe440=
|
|
ENST00000617423.4:c.705C>T
|
ENSP00000478688.1:p.Phe235=
|
|
NM_000488.3:c.1320C>T , LRG_577t1:c.1320C>T
|
NP_000479.1:p.Phe440=
|
|
XM_005245198.2:c.1176C>T
|
XP_005245255.1:p.Phe392=
|
|
NM_001365052.1:c.1176C>T
|
NP_001351981.1:p.Phe392=
|
|
NM_000488.4:c.1320C>T
MANE Select
|
NP_000479.1:p.Phe440=
|
|
NM_001365052.2:c.1176C>T
|
NP_001351981.1:p.Phe392=
|
|
NM_001386302.1:c.1443C>T
|
NP_001373231.1:p.Phe481=
|
|
NM_001386303.1:c.1401C>T
|
NP_001373232.1:p.Phe467=
|
|
NM_001386304.1:c.1299C>T
|
NP_001373233.1:p.Phe433=
|
|
NM_001386305.1:c.1263C>T
|
NP_001373234.1:p.Phe421=
|
|
NM_001386306.1:c.1104C>T
|
NP_001373235.1:p.Phe368=
|
|