ENST00000696192.1:c.*401C>G
(F12)
|
ENSP00000512476.1:n.*401C>G
|
|
ENST00000696193.1:c.*1105C>G
(F12)
|
ENSP00000512477.1:n.*1105C>G
|
|
ENST00000696194.1:c.*325C>G
(F12)
|
ENSP00000512478.1:n.*325C>G
|
|
ENST00000696195.1:n.3538C>G
(F12)
|
|
|
ENST00000696200.1:n.838C>G
(F12)
|
|
|
ENST00000696201.1:c.735C>G
(F12)
|
ENSP00000512482.1:p.Ala245=
|
|
ENST00000253496.4:c.735C>G
(F12)
MANE Select
|
ENSP00000253496.3:p.Ala245=
|
|
ENST00000253496.3:c.735C>G
(F12)
|
ENSP00000253496.3:p.Ala245=
|
|
ENST00000502598.5:c.-45+1038G>C
(GRK6)
|
ENSP00000422873.1:n.-45+1038G>C
|
|
ENST00000503736.1:n.173-151C>G
(F12)
|
|
|
ENST00000506296.5:c.-45+7G>C
(GRK6)
|
ENSP00000421055.1:n.-45+7G>C
|
|
NM_000505.3:c.735C>G , LRG_145t1:c.735C>G
(F12)
|
NP_000496.2:p.Ala245=
|
|
XM_011534461.1:c.735C>G
(F12)
|
XP_011532763.1:p.Ala245=
|
|
XM_011534462.1:c.399C>G
(F12)
|
XP_011532764.1:p.Ala133=
|
|
XM_011534462.2:c.399C>G
(F12)
|
XP_011532764.1:p.Ala133=
|
|
XM_017009773.2:c.1417-7200G>C
(SLC34A1)
|
XP_016865262.1:n.1417-7200G>C
|
|
NM_000505.4:c.735C>G
(F12)
MANE Select
|
NP_000496.2:p.Ala245=
|
|