ENST00000696192.1:c.*285G>T
(F12)
|
ENSP00000512476.1:n.*285G>T
|
|
ENST00000696193.1:c.*844G>T
(F12)
|
ENSP00000512477.1:n.*844G>T
|
|
ENST00000696194.1:c.*209G>T
(F12)
|
ENSP00000512478.1:n.*209G>T
|
|
ENST00000696195.1:n.3277G>T
(F12)
|
|
|
ENST00000696200.1:n.722G>T
(F12)
|
|
|
ENST00000696201.1:c.619G>T
(F12)
|
ENSP00000512482.1:p.Ala207Ser
|
|
ENST00000253496.4:c.619G>T
(F12)
MANE Select
|
ENSP00000253496.3:p.Ala207Ser
|
|
ENST00000253496.3:c.619G>T
(F12)
|
ENSP00000253496.3:p.Ala207Ser
|
|
ENST00000502598.5:c.-45+1299C>A
(GRK6)
|
ENSP00000422873.1:n.-45+1299C>A
|
|
ENST00000503736.1:n.157G>T
(F12)
|
|
|
ENST00000506296.5:c.-45+268C>A
(GRK6)
|
ENSP00000421055.1:n.-45+268C>A
|
|
NM_000505.3:c.619G>T , LRG_145t1:c.619G>T
(F12)
|
NP_000496.2:p.Ala207Ser
|
|
XM_011534461.1:c.619G>T
(F12)
|
XP_011532763.1:p.Ala207Ser
|
|
XM_011534462.1:c.283G>T
(F12)
|
XP_011532764.1:p.Ala95Ser
|
|
XM_011534462.2:c.283G>T
(F12)
|
XP_011532764.1:p.Ala95Ser
|
|
XM_017009773.2:c.1417-6939C>A
(SLC34A1)
|
XP_016865262.1:n.1417-6939C>A
|
|
NM_000505.4:c.619G>T
(F12)
MANE Select
|
NP_000496.2:p.Ala207Ser
|
|