ENST00000696192.1:c.*633C>G
(F12)
|
ENSP00000512476.1:n.*633C>G
|
|
ENST00000696193.1:c.*1337C>G
(F12)
|
ENSP00000512477.1:n.*1337C>G
|
|
ENST00000696194.1:c.*557C>G
(F12)
|
ENSP00000512478.1:n.*557C>G
|
|
ENST00000696195.1:n.3770C>G
(F12)
|
|
|
ENST00000696200.1:n.1070C>G
(F12)
|
|
|
ENST00000696201.1:c.967C>G
(F12)
|
ENSP00000512482.1:p.Pro323Ala
|
|
ENST00000253496.4:c.967C>G
(F12)
MANE Select
|
ENSP00000253496.3:p.Pro323Ala
|
|
ENST00000253496.3:c.967C>G
(F12)
|
ENSP00000253496.3:p.Pro323Ala
|
|
ENST00000502598.5:c.-45+721G>C
(GRK6)
|
ENSP00000422873.1:n.-45+721G>C
|
|
ENST00000502854.5:n.226C>G
(F12)
|
|
|
ENST00000503736.1:n.339C>G
(F12)
|
|
|
ENST00000510358.5:n.226C>G
(F12)
|
|
|
NM_000505.3:c.967C>G , LRG_145t1:c.967C>G
(F12)
|
NP_000496.2:p.Pro323Ala
|
|
XM_011534461.1:c.967C>G
(F12)
|
XP_011532763.1:p.Pro323Ala
|
|
XM_011534462.1:c.631C>G
(F12)
|
XP_011532764.1:p.Pro211Ala
|
|
XM_011534462.2:c.631C>G
(F12)
|
XP_011532764.1:p.Pro211Ala
|
|
XM_017009773.2:c.1416+7173G>C
(SLC34A1)
|
XP_016865262.1:n.1416+7173G>C
|
|
NM_000505.4:c.967C>G
(F12)
MANE Select
|
NP_000496.2:p.Pro323Ala
|
|