NM_015141.4:c.216A>T
MANE Select
|
NP_055956.1:p.Pro72=
|
ENST00000282541.10:c.216A>T
MANE Select
|
ENSP00000282541.6:p.Pro72=
|
NM_015141.3:c.216A>T , LRG_419t1:c.216A>T
|
NP_055956.1:p.Pro72=
|
ENST00000282541.9:c.216A>T
|
ENSP00000282541.5:p.Pro72=
|
ENST00000425459.5:c.216A>T
|
ENSP00000408770.1:p.Pro72=
|
ENST00000428684.1:c.48-10343A>T
|
ENSP00000392199.1:n.48-10343A>T
|
ENST00000429432.5:c.99A>T
|
ENSP00000393861.1:p.Pro33=
|
ENST00000431009.1:c.99A>T
|
ENSP00000416518.1:p.Pro33=
|
XM_005264983.2:c.216A>T
|
XP_005265040.1:p.Pro72=
|
XM_006713068.2:c.216A>T
|
XP_006713131.1:p.Pro72=
|