ENST00000497571.6:c.366G>T
MANE Select
|
ENSP00000419923.1:p.Thr122=
|
|
ENST00000173785.4:n.101G>T
|
|
|
ENST00000380946.3:n.601G>T
|
|
|
ENST00000469435.1:c.366G>T
|
ENSP00000419079.1:p.Thr122=
|
|
ENST00000497571.5:c.366G>T
|
ENSP00000419923.1:p.Thr122=
|
|
ENST00000542957.1:c.366G>T
|
ENSP00000445301.1:p.Thr122=
|
|
NM_001160124.1:c.366G>T
|
NP_001153596.1:p.Thr122=
|
|
NM_001160125.1:c.366G>T
|
NP_001153597.1:p.Thr122=
|
|
NM_001300.5:c.366G>T
|
NP_001291.3:p.Thr122=
|
|
NR_027653.1:n.633G>T
|
|
|
NM_001300.6:c.366G>T
MANE Select
|
NP_001291.3:p.Thr122=
|
|
NM_001160124.2:c.366G>T
|
NP_001153596.1:p.Thr122=
|
|
NR_027653.2:n.561G>T
|
|
|
NM_001160125.2:c.366G>T
|
NP_001153597.1:p.Thr122=
|
|