ENST00000415738.3:c.970G>A
MANE Select
|
ENSP00000406998.2:p.Gly324Ser
|
|
ENST00000339711.8:c.970G>A
|
ENSP00000339764.4:p.Gly324Ser
|
|
ENST00000415738.2:c.970G>A
|
ENSP00000406998.2:p.Gly324Ser
|
|
ENST00000504452.5:c.970G>A
|
ENSP00000423985.1:p.Gly324Ser
|
|
ENST00000515013.5:c.970G>A
|
ENSP00000425149.1:p.Gly324Ser
|
|
NM_001099403.1:c.970G>A
|
NP_001092873.1:p.Gly324Ser
|
|
NM_020226.3:c.970G>A
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NP_064611.3:p.Gly324Ser
|
|
XM_005263144.2:c.973G>A
|
XP_005263201.1:p.Gly325Ser
|
|
XM_005263145.2:c.973G>A
|
XP_005263202.1:p.Gly325Ser
|
|
XM_005263146.3:c.970G>A
|
XP_005263203.1:p.Gly324Ser
|
|
XM_011532133.1:c.1813G>A
|
XP_011530435.1:p.Gly605Ser
|
|
XM_011532134.1:c.1810G>A
|
XP_011530436.1:p.Gly604Ser
|
|
XM_011532135.1:c.1672G>A
|
XP_011530437.1:p.Gly558Ser
|
|
XM_011532136.1:c.1525G>A
|
XP_011530438.1:p.Gly509Ser
|
|
XM_011532137.1:c.1525G>A
|
XP_011530439.1:p.Gly509Ser
|
|
XM_011532138.1:c.1525G>A
|
XP_011530440.1:p.Gly509Ser
|
|
XM_011532139.1:c.1525G>A
|
XP_011530441.1:p.Gly509Ser
|
|
XM_011532140.1:c.1525G>A
|
XP_011530442.1:p.Gly509Ser
|
|
XM_011532141.1:c.1387G>A
|
XP_011530443.1:p.Gly463Ser
|
|
XM_011532142.1:c.1366G>A
|
XP_011530444.1:p.Gly456Ser
|
|
XM_005263146.4:c.970G>A
|
XP_005263203.1:p.Gly324Ser
|
|
XM_011532133.2:c.1813G>A
|
XP_011530435.1:p.Gly605Ser
|
|
XM_011532135.2:c.1672G>A
|
XP_011530437.1:p.Gly558Ser
|
|
XM_011532140.2:c.1525G>A
|
XP_011530442.1:p.Gly509Ser
|
|
XM_011532141.3:c.1387G>A
|
XP_011530443.1:p.Gly463Ser
|
|
XM_017008468.1:c.1522G>A
|
XP_016863957.1:p.Gly508Ser
|
|
XM_017008469.1:c.1609G>A
|
XP_016863958.1:p.Gly537Ser
|
|
XM_017008470.1:c.1525G>A
|
XP_016863959.1:p.Gly509Ser
|
|
NM_001099403.2:c.970G>A
MANE Select
|
NP_001092873.1:p.Gly324Ser
|
|
NM_020226.4:c.970G>A
|
NP_064611.3:p.Gly324Ser
|
|