ENST00000415738.3:c.980C>A
MANE Select
|
ENSP00000406998.2:p.Ala327Asp
|
|
ENST00000339711.8:c.980C>A
|
ENSP00000339764.4:p.Ala327Asp
|
|
ENST00000415738.2:c.980C>A
|
ENSP00000406998.2:p.Ala327Asp
|
|
ENST00000504452.5:c.980C>A
|
ENSP00000423985.1:p.Ala327Asp
|
|
ENST00000515013.5:c.980C>A
|
ENSP00000425149.1:p.Ala327Asp
|
|
NM_001099403.1:c.980C>A
|
NP_001092873.1:p.Ala327Asp
|
|
NM_020226.3:c.980C>A
|
NP_064611.3:p.Ala327Asp
|
|
XM_005263144.2:c.983C>A
|
XP_005263201.1:p.Ala328Asp
|
|
XM_005263145.2:c.983C>A
|
XP_005263202.1:p.Ala328Asp
|
|
XM_005263146.3:c.980C>A
|
XP_005263203.1:p.Ala327Asp
|
|
XM_011532133.1:c.1823C>A
|
XP_011530435.1:p.Ala608Asp
|
|
XM_011532134.1:c.1820C>A
|
XP_011530436.1:p.Ala607Asp
|
|
XM_011532135.1:c.1682C>A
|
XP_011530437.1:p.Ala561Asp
|
|
XM_011532136.1:c.1535C>A
|
XP_011530438.1:p.Ala512Asp
|
|
XM_011532137.1:c.1535C>A
|
XP_011530439.1:p.Ala512Asp
|
|
XM_011532138.1:c.1535C>A
|
XP_011530440.1:p.Ala512Asp
|
|
XM_011532139.1:c.1535C>A
|
XP_011530441.1:p.Ala512Asp
|
|
XM_011532140.1:c.1535C>A
|
XP_011530442.1:p.Ala512Asp
|
|
XM_011532141.1:c.1397C>A
|
XP_011530443.1:p.Ala466Asp
|
|
XM_011532142.1:c.1376C>A
|
XP_011530444.1:p.Ala459Asp
|
|
XM_005263146.4:c.980C>A
|
XP_005263203.1:p.Ala327Asp
|
|
XM_011532133.2:c.1823C>A
|
XP_011530435.1:p.Ala608Asp
|
|
XM_011532135.2:c.1682C>A
|
XP_011530437.1:p.Ala561Asp
|
|
XM_011532140.2:c.1535C>A
|
XP_011530442.1:p.Ala512Asp
|
|
XM_011532141.3:c.1397C>A
|
XP_011530443.1:p.Ala466Asp
|
|
XM_017008468.1:c.1532C>A
|
XP_016863957.1:p.Ala511Asp
|
|
XM_017008469.1:c.1619C>A
|
XP_016863958.1:p.Ala540Asp
|
|
XM_017008470.1:c.1535C>A
|
XP_016863959.1:p.Ala512Asp
|
|
NM_001099403.2:c.980C>A
MANE Select
|
NP_001092873.1:p.Ala327Asp
|
|
NM_020226.4:c.980C>A
|
NP_064611.3:p.Ala327Asp
|
|