ENST00000367400.8:c.2938T>G
MANE Select
|
ENSP00000356370.3:p.Phe980Val
|
|
ENST00000638467.1:c.2938T>G
|
ENSP00000491102.1:p.Phe980Val
|
|
ENST00000681519.1:c.1819T>G
|
ENSP00000505267.1:p.Phe607Val
|
|
ENST00000367397.1:c.1081T>G
|
ENSP00000356367.1:p.Phe361Val
|
|
ENST00000367399.6:c.2602T>G
|
ENSP00000356369.2:p.Phe868Val
|
|
ENST00000367400.7:c.2938T>G
|
ENSP00000356370.3:p.Phe980Val
|
|
ENST00000484075.5:c.2938T>G
|
ENSP00000433932.1:p.Phe980Val
|
|
ENST00000535699.5:c.2866T>G
|
ENSP00000438786.1:p.Phe956Val
|
|
ENST00000538660.5:c.2129-799T>G
|
ENSP00000438091.1:n.2129-799T>G
|
|
NM_001193640.1:c.2602T>G
|
NP_001180569.1:p.Phe868Val
|
|
NM_001257965.1:c.2866T>G
|
NP_001244894.1:p.Phe956Val
|
|
NM_001257966.1:c.2129-799T>G
|
NP_001244895.1:n.2129-799T>G
|
|
NM_201253.2:c.2938T>G
|
NP_957705.1:p.Phe980Val
|
|
NR_047563.1:n.2939T>G
|
|
|
NR_047564.1:n.3147T>G
|
|
|
XM_011509365.1:c.2938T>G
|
XP_011507667.1:p.Phe980Val
|
|
XM_011509366.1:c.2938T>G
|
XP_011507668.1:p.Phe980Val
|
|
XM_011509367.1:c.2938T>G
|
XP_011507669.1:p.Phe980Val
|
|
XM_011509368.1:c.2356T>G
|
XP_011507670.1:p.Phe786Val
|
|
XM_011509369.1:c.1381T>G
|
XP_011507671.1:p.Phe461Val
|
|
XM_011509365.2:c.2938T>G
|
XP_011507667.1:p.Phe980Val
|
|
XM_011509369.2:c.1381T>G
|
XP_011507671.1:p.Phe461Val
|
|
XM_017000851.1:c.2095T>G
|
XP_016856340.1:p.Phe699Val
|
|
XM_017000852.1:c.3073T>G
|
XP_016856341.1:p.Phe1025Val
|
|
NM_201253.3:c.2938T>G
MANE Select
|
NP_957705.1:p.Phe980Val
|
|
NM_001193640.2:c.2602T>G
|
NP_001180569.1:p.Phe868Val
|
|
NM_001257965.2:c.2866T>G
|
NP_001244894.1:p.Phe956Val
|
|
NR_047563.2:n.2891T>G
|
|
|
NR_047564.2:n.3099T>G
|
|
|
NM_001257966.2:c.2129-799T>G
|
NP_001244895.1:n.2129-799T>G
|
|