|
ENST00000415738.3:c.1085T>C
MANE Select
|
ENSP00000406998.2:p.Phe362Ser
|
|
|
ENST00000339711.8:c.1085T>C
|
ENSP00000339764.4:p.Phe362Ser
|
|
|
ENST00000415738.2:c.1085T>C
|
ENSP00000406998.2:p.Phe362Ser
|
|
|
ENST00000504452.5:c.1085T>C
|
ENSP00000423985.1:p.Phe362Ser
|
|
|
ENST00000515013.5:c.1085T>C
|
ENSP00000425149.1:p.Phe362Ser
|
|
|
NM_001099403.1:c.1085T>C
|
NP_001092873.1:p.Phe362Ser
|
|
|
NM_020226.3:c.1085T>C
|
NP_064611.3:p.Phe362Ser
|
|
|
XM_005263144.2:c.1088T>C
|
XP_005263201.1:p.Phe363Ser
|
|
|
XM_005263145.2:c.1088T>C
|
XP_005263202.1:p.Phe363Ser
|
|
|
XM_005263146.3:c.1085T>C
|
XP_005263203.1:p.Phe362Ser
|
|
|
XM_011532133.1:c.1928T>C
|
XP_011530435.1:p.Phe643Ser
|
|
|
XM_011532134.1:c.1925T>C
|
XP_011530436.1:p.Phe642Ser
|
|
|
XM_011532135.1:c.1787T>C
|
XP_011530437.1:p.Phe596Ser
|
|
|
XM_011532136.1:c.1640T>C
|
XP_011530438.1:p.Phe547Ser
|
|
|
XM_011532137.1:c.1640T>C
|
XP_011530439.1:p.Phe547Ser
|
|
|
XM_011532138.1:c.1640T>C
|
XP_011530440.1:p.Phe547Ser
|
|
|
XM_011532139.1:c.1640T>C
|
XP_011530441.1:p.Phe547Ser
|
|
|
XM_011532140.1:c.1640T>C
|
XP_011530442.1:p.Phe547Ser
|
|
|
XM_011532141.1:c.1502T>C
|
XP_011530443.1:p.Phe501Ser
|
|
|
XM_011532142.1:c.1481T>C
|
XP_011530444.1:p.Phe494Ser
|
|
|
XM_005263146.4:c.1085T>C
|
XP_005263203.1:p.Phe362Ser
|
|
|
XM_011532133.2:c.1928T>C
|
XP_011530435.1:p.Phe643Ser
|
|
|
XM_011532135.2:c.1787T>C
|
XP_011530437.1:p.Phe596Ser
|
|
|
XM_011532140.2:c.1640T>C
|
XP_011530442.1:p.Phe547Ser
|
|
|
XM_011532141.3:c.1502T>C
|
XP_011530443.1:p.Phe501Ser
|
|
|
XM_017008468.1:c.1637T>C
|
XP_016863957.1:p.Phe546Ser
|
|
|
XM_017008469.1:c.1724T>C
|
XP_016863958.1:p.Phe575Ser
|
|
|
XM_017008470.1:c.1640T>C
|
XP_016863959.1:p.Phe547Ser
|
|
|
NM_001099403.2:c.1085T>C
MANE Select
|
NP_001092873.1:p.Phe362Ser
|
|
|
NM_020226.4:c.1085T>C
|
NP_064611.3:p.Phe362Ser
|
|
