ENST00000480266.6:c.654T>C
|
ENSP00000479015.1:p.Gly218=
|
|
ENST00000373203.9:c.1200T>C
MANE Select
|
ENSP00000362299.4:p.Gly400=
|
|
ENST00000344849.4:c.1200T>C
|
ENSP00000341917.3:p.Gly400=
|
|
ENST00000373203.8:c.1200T>C
|
ENSP00000362299.4:p.Gly400=
|
|
ENST00000480266.5:c.654T>C
|
ENSP00000479015.1:p.Gly218=
|
|
ENST00000486329.1:n.168T>C
|
|
|
NM_000118.3:c.1200T>C , LRG_589t1:c.1200T>C
|
NP_000109.1:p.Gly400=
|
|
NM_001114753.2:c.1200T>C , LRG_589t2:c.1200T>C
|
NP_001108225.1:p.Gly400=
|
|
NM_001278138.1:c.654T>C
|
NP_001265067.1:p.Gly218=
|
|
NR_136302.1:n.1569-1223A>G
|
|
|
NM_001114753.3:c.1200T>C
MANE Select
|
NP_001108225.1:p.Gly400=
|
|
NM_001278138.2:c.654T>C
|
NP_001265067.1:p.Gly218=
|
|