ENST00000696192.1:c.*471C>T
(F12)
|
ENSP00000512476.1:n.*471C>T
|
|
ENST00000696193.1:c.*1175C>T
(F12)
|
ENSP00000512477.1:n.*1175C>T
|
|
ENST00000696194.1:c.*395C>T
(F12)
|
ENSP00000512478.1:n.*395C>T
|
|
ENST00000696195.1:n.3608C>T
(F12)
|
|
|
ENST00000696200.1:n.908C>T
(F12)
|
|
|
ENST00000696201.1:c.805C>T
(F12)
|
ENSP00000512482.1:p.Pro269Ser
|
|
ENST00000253496.4:c.805C>T
(F12)
MANE Select
|
ENSP00000253496.3:p.Pro269Ser
|
|
ENST00000253496.3:c.805C>T
(F12)
|
ENSP00000253496.3:p.Pro269Ser
|
|
ENST00000502598.5:c.-45+883G>A
(GRK6)
|
ENSP00000422873.1:n.-45+883G>A
|
|
ENST00000502854.5:n.64C>T
(F12)
|
|
|
ENST00000503736.1:n.177C>T
(F12)
|
|
|
ENST00000506296.5:c.-193G>A
(GRK6)
|
ENSP00000421055.1:n.-193G>A
|
|
ENST00000510358.5:n.64C>T
(F12)
|
|
|
NM_000505.3:c.805C>T , LRG_145t1:c.805C>T
(F12)
|
NP_000496.2:p.Pro269Ser
|
|
XM_011534461.1:c.805C>T
(F12)
|
XP_011532763.1:p.Pro269Ser
|
|
XM_011534462.1:c.469C>T
(F12)
|
XP_011532764.1:p.Pro157Ser
|
|
XM_011534462.2:c.469C>T
(F12)
|
XP_011532764.1:p.Pro157Ser
|
|
XM_017009773.2:c.1416+7335G>A
(SLC34A1)
|
XP_016865262.1:n.1416+7335G>A
|
|
NM_000505.4:c.805C>T
(F12)
MANE Select
|
NP_000496.2:p.Pro269Ser
|
|