ENST00000367698.4:c.1361T>C
MANE Select
|
ENSP00000356671.3:p.Phe454Ser
|
|
ENST00000367698.3:c.1361T>C
|
ENSP00000356671.3:p.Phe454Ser
|
|
ENST00000617423.4:c.746T>C
|
ENSP00000478688.1:p.Phe249Ser
|
|
NM_000488.3:c.1361T>C , LRG_577t1:c.1361T>C
|
NP_000479.1:p.Phe454Ser
|
|
XM_005245198.2:c.1217T>C
|
XP_005245255.1:p.Phe406Ser
|
|
NM_001365052.1:c.1217T>C
|
NP_001351981.1:p.Phe406Ser
|
|
NM_000488.4:c.1361T>C
MANE Select
|
NP_000479.1:p.Phe454Ser
|
|
NM_001365052.2:c.1217T>C
|
NP_001351981.1:p.Phe406Ser
|
|
NM_001386302.1:c.1484T>C
|
NP_001373231.1:p.Phe495Ser
|
|
NM_001386303.1:c.1442T>C
|
NP_001373232.1:p.Phe481Ser
|
|
NM_001386304.1:c.1340T>C
|
NP_001373233.1:p.Phe447Ser
|
|
NM_001386305.1:c.1304T>C
|
NP_001373234.1:p.Phe435Ser
|
|
NM_001386306.1:c.1145T>C
|
NP_001373235.1:p.Phe382Ser
|
|