ENST00000236959.14:c.326C>G
MANE Select
|
ENSP00000236959.9:p.Thr109Arg
|
|
ENST00000236959.13:c.326C>G
|
ENSP00000236959.9:p.Thr109Arg
|
|
ENST00000413174.1:c.149C>G
|
ENSP00000402393.1:p.Thr50Arg
|
|
ENST00000427397.5:c.*376C>G
|
ENSP00000394317.1:n.*376C>G
|
|
ENST00000435675.5:c.323C>G
|
ENSP00000415935.1:p.Thr108Arg
|
|
ENST00000443953.5:c.*423C>G
|
ENSP00000406792.1:n.*423C>G
|
|
ENST00000444305.5:c.*4C>G
|
ENSP00000388675.1:n.*4C>G
|
|
ENST00000488712.5:n.538C>G
|
|
|
NM_004044.6:c.326C>G
|
NP_004035.2:p.Thr109Arg
|
|
XM_017004187.2:c.326C>G
|
XP_016859676.1:p.Thr109Arg
|
|
XM_024452919.1:c.149C>G
|
XP_024308687.1:p.Thr50Arg
|
|
NM_004044.7:c.326C>G
MANE Select
|
NP_004035.2:p.Thr109Arg
|
|