ENST00000696192.1:c.*466+38G>A
(F12)
|
ENSP00000512476.1:n.*466+38G>A
|
|
ENST00000696193.1:c.*1170+38G>A
(F12)
|
ENSP00000512477.1:n.*1170+38G>A
|
|
ENST00000696194.1:c.*390+38G>A
(F12)
|
ENSP00000512478.1:n.*390+38G>A
|
|
ENST00000696195.1:n.3603+38G>A
(F12)
|
|
|
ENST00000696200.1:n.903+38G>A
(F12)
|
|
|
ENST00000696201.1:c.800+38G>A
(F12)
|
ENSP00000512482.1:n.800+38G>A
|
|
ENST00000253496.4:c.800+38G>A
(F12)
MANE Select
|
ENSP00000253496.3:n.800+38G>A
|
|
ENST00000253496.3:c.800+38G>A
(F12)
|
ENSP00000253496.3:n.800+38G>A
|
|
ENST00000502598.5:c.-45+935C>T
(GRK6)
|
ENSP00000422873.1:n.-45+935C>T
|
|
ENST00000502854.5:n.12G>A
(F12)
|
|
|
ENST00000503736.1:n.173-48G>A
(F12)
|
|
|
ENST00000506296.5:c.-141C>T
(GRK6)
|
ENSP00000421055.1:n.-141C>T
|
|
ENST00000510358.5:n.12G>A
(F12)
|
|
|
NM_000505.3:c.800+38G>A , LRG_145t1:c.800+38G>A
(F12)
|
NP_000496.2:n.800+38G>A
|
|
XM_011534461.1:c.800+38G>A
(F12)
|
XP_011532763.1:n.800+38G>A
|
|
XM_011534462.1:c.464+38G>A
(F12)
|
XP_011532764.1:n.464+38G>A
|
|
XM_011534462.2:c.464+38G>A
(F12)
|
XP_011532764.1:n.464+38G>A
|
|
XM_017009773.2:c.1417-7303C>T
(SLC34A1)
|
XP_016865262.1:n.1417-7303C>T
|
|
NM_000505.4:c.800+38G>A
(F12)
MANE Select
|
NP_000496.2:n.800+38G>A
|
|