ENST00000696192.1:c.*543G>T
(F12)
|
ENSP00000512476.1:n.*543G>T
|
|
ENST00000696193.1:c.*1247G>T
(F12)
|
ENSP00000512477.1:n.*1247G>T
|
|
ENST00000696194.1:c.*467G>T
(F12)
|
ENSP00000512478.1:n.*467G>T
|
|
ENST00000696195.1:n.3680G>T
(F12)
|
|
|
ENST00000696200.1:n.980G>T
(F12)
|
|
|
ENST00000696201.1:c.877G>T
(F12)
|
ENSP00000512482.1:p.Ala293Ser
|
|
ENST00000253496.4:c.877G>T
(F12)
MANE Select
|
ENSP00000253496.3:p.Ala293Ser
|
|
ENST00000253496.3:c.877G>T
(F12)
|
ENSP00000253496.3:p.Ala293Ser
|
|
ENST00000502598.5:c.-45+811C>A
(GRK6)
|
ENSP00000422873.1:n.-45+811C>A
|
|
ENST00000502854.5:n.136G>T
(F12)
|
|
|
ENST00000503736.1:n.249G>T
(F12)
|
|
|
ENST00000510358.5:n.136G>T
(F12)
|
|
|
NM_000505.3:c.877G>T , LRG_145t1:c.877G>T
(F12)
|
NP_000496.2:p.Ala293Ser
|
|
XM_011534461.1:c.877G>T
(F12)
|
XP_011532763.1:p.Ala293Ser
|
|
XM_011534462.1:c.541G>T
(F12)
|
XP_011532764.1:p.Ala181Ser
|
|
XM_011534462.2:c.541G>T
(F12)
|
XP_011532764.1:p.Ala181Ser
|
|
XM_017009773.2:c.1416+7263C>A
(SLC34A1)
|
XP_016865262.1:n.1416+7263C>A
|
|
NM_000505.4:c.877G>T
(F12)
MANE Select
|
NP_000496.2:p.Ala293Ser
|
|