ENST00000223051.8:c.2329G>T
MANE Select
|
ENSP00000223051.3:p.Ala777Ser
|
|
ENST00000223051.7:c.2329G>T
|
ENSP00000223051.3:p.Ala777Ser
|
|
ENST00000431692.5:c.*1004G>T
|
ENSP00000413905.1:n.*1004G>T
|
|
ENST00000462090.5:n.1365G>T
|
|
|
ENST00000462107.1:c.2329G>T
|
ENSP00000420525.1:p.Ala777Ser
|
|
ENST00000465294.5:n.2249G>T
|
|
|
ENST00000476304.5:n.1950G>T
|
|
|
ENST00000490084.5:c.1682G>T
|
|
|
NM_001206855.1:c.1816G>T
|
NP_001193784.1:p.Ala606Ser
|
|
NM_003227.3:c.2329G>T
|
NP_003218.2:p.Ala777Ser
|
|
XM_005250553.3:c.2329G>T
|
XP_005250610.1:p.Ala777Ser
|
|
NM_001206855.2:c.1816G>T
|
NP_001193784.1:p.Ala606Ser
|
|
XM_005250553.4:c.2329G>T
|
XP_005250610.1:p.Ala777Ser
|
|
XM_017012573.1:c.2329G>T
|
XP_016868062.1:p.Ala777Ser
|
|
NM_003227.4:c.2329G>T
MANE Select
|
NP_003218.2:p.Ala777Ser
|
|
NM_001206855.3:c.1816G>T
|
NP_001193784.1:p.Ala606Ser
|
|