ENST00000415738.3:c.1040A>C
MANE Select
|
ENSP00000406998.2:p.Asp347Ala
|
|
ENST00000339711.8:c.1040A>C
|
ENSP00000339764.4:p.Asp347Ala
|
|
ENST00000415738.2:c.1040A>C
|
ENSP00000406998.2:p.Asp347Ala
|
|
ENST00000504452.5:c.1040A>C
|
ENSP00000423985.1:p.Asp347Ala
|
|
ENST00000515013.5:c.1040A>C
|
ENSP00000425149.1:p.Asp347Ala
|
|
NM_001099403.1:c.1040A>C
|
NP_001092873.1:p.Asp347Ala
|
|
NM_020226.3:c.1040A>C
|
NP_064611.3:p.Asp347Ala
|
|
XM_005263144.2:c.1043A>C
|
XP_005263201.1:p.Asp348Ala
|
|
XM_005263145.2:c.1043A>C
|
XP_005263202.1:p.Asp348Ala
|
|
XM_005263146.3:c.1040A>C
|
XP_005263203.1:p.Asp347Ala
|
|
XM_011532133.1:c.1883A>C
|
XP_011530435.1:p.Asp628Ala
|
|
XM_011532134.1:c.1880A>C
|
XP_011530436.1:p.Asp627Ala
|
|
XM_011532135.1:c.1742A>C
|
XP_011530437.1:p.Asp581Ala
|
|
XM_011532136.1:c.1595A>C
|
XP_011530438.1:p.Asp532Ala
|
|
XM_011532137.1:c.1595A>C
|
XP_011530439.1:p.Asp532Ala
|
|
XM_011532138.1:c.1595A>C
|
XP_011530440.1:p.Asp532Ala
|
|
XM_011532139.1:c.1595A>C
|
XP_011530441.1:p.Asp532Ala
|
|
XM_011532140.1:c.1595A>C
|
XP_011530442.1:p.Asp532Ala
|
|
XM_011532141.1:c.1457A>C
|
XP_011530443.1:p.Asp486Ala
|
|
XM_011532142.1:c.1436A>C
|
XP_011530444.1:p.Asp479Ala
|
|
XM_005263146.4:c.1040A>C
|
XP_005263203.1:p.Asp347Ala
|
|
XM_011532133.2:c.1883A>C
|
XP_011530435.1:p.Asp628Ala
|
|
XM_011532135.2:c.1742A>C
|
XP_011530437.1:p.Asp581Ala
|
|
XM_011532140.2:c.1595A>C
|
XP_011530442.1:p.Asp532Ala
|
|
XM_011532141.3:c.1457A>C
|
XP_011530443.1:p.Asp486Ala
|
|
XM_017008468.1:c.1592A>C
|
XP_016863957.1:p.Asp531Ala
|
|
XM_017008469.1:c.1679A>C
|
XP_016863958.1:p.Asp560Ala
|
|
XM_017008470.1:c.1595A>C
|
XP_016863959.1:p.Asp532Ala
|
|
NM_001099403.2:c.1040A>C
MANE Select
|
NP_001092873.1:p.Asp347Ala
|
|
NM_020226.4:c.1040A>C
|
NP_064611.3:p.Asp347Ala
|
|