ENST00000684880.1:c.*273T>G
|
ENSP00000510280.1:n.*273T>G
|
|
ENST00000689310.1:c.637T>G
|
ENSP00000510438.1:p.Phe213Val
|
|
ENST00000370818.8:c.685T>G
MANE Select
|
ENSP00000359854.3:p.Phe229Val
|
|
ENST00000394299.7:c.685T>G
|
ENSP00000377836.2:p.Phe229Val
|
|
ENST00000370818.7:c.685T>G
|
ENSP00000359854.3:p.Phe229Val
|
|
ENST00000394299.6:c.685T>G
|
ENSP00000377836.2:p.Phe229Val
|
|
ENST00000631057.2:c.523T>G
|
ENSP00000486325.1:p.Phe175Val
|
|
NM_001164617.1:c.685T>G
|
NP_001158089.1:p.Phe229Val
|
|
NM_001164618.1:c.637T>G
|
NP_001158090.1:p.Phe213Val
|
|
NM_001164619.1:c.523T>G
|
NP_001158091.1:p.Phe175Val
|
|
NM_004484.3:c.685T>G , LRG_505t1:c.685T>G
|
NP_004475.1:p.Phe229Val
|
|
XM_017029413.2:c.685T>G
|
XP_016884902.1:p.Phe229Val
|
|
NM_001164617.2:c.685T>G
|
NP_001158089.1:p.Phe229Val
|
|
NM_001164618.2:c.637T>G
|
NP_001158090.1:p.Phe213Val
|
|
NM_001164619.2:c.523T>G
|
NP_001158091.1:p.Phe175Val
|
|
NM_004484.4:c.685T>G
MANE Select
|
NP_004475.1:p.Phe229Val
|
|