ENST00000221930.6:c.828C>T
MANE Select
|
ENSP00000221930.4:p.His276=
|
|
ENST00000600196.2:c.712+255C>T
|
ENSP00000504008.1:n.712+255C>T
|
|
ENST00000677934.1:c.634+2832C>T
|
ENSP00000504769.1:n.634+2832C>T
|
|
ENST00000221930.5:c.828C>T
|
ENSP00000221930.4:p.His276=
|
|
ENST00000598758.5:c.116C>T
|
|
|
ENST00000600196.1:n.172+255C>T
|
|
|
NM_000660.5:c.828C>T
|
NP_000651.3:p.His276=
|
|
XM_011527242.1:c.831C>T
|
XP_011525544.1:p.His277=
|
|
NM_000660.6:c.828C>T
|
NP_000651.3:p.His276=
|
|
XM_011527242.2:c.831C>T
|
XP_011525544.1:p.His277=
|
|
NM_000660.7:c.828C>T
MANE Select
|
NP_000651.3:p.His276=
|
|