ENST00000241453.12:c.2498C>A
MANE Select
|
ENSP00000241453.7:p.Ala833Asp
|
|
ENST00000241453.11:c.2498C>A
|
ENSP00000241453.7:p.Ala833Asp
|
|
ENST00000380987.2:c.*410C>A
|
ENSP00000370374.2:n.*410C>A
|
|
NM_004119.2:c.2498C>A , LRG_457t1:c.2498C>A
|
NP_004110.2:p.Ala833Asp
|
|
NR_130706.1:n.2712C>A
|
|
|
XM_011535015.1:c.2441C>A
|
XP_011533317.1:p.Ala814Asp
|
|
XM_011535016.1:c.1973C>A
|
XP_011533318.1:p.Ala658Asp
|
|
XM_011535017.1:c.1973C>A
|
XP_011533319.1:p.Ala658Asp
|
|
XM_011535018.1:c.1973C>A
|
XP_011533320.1:p.Ala658Asp
|
|
XM_011535015.2:c.2441C>A
|
XP_011533317.1:p.Ala814Asp
|
|
XM_011535017.2:c.1973C>A
|
XP_011533319.1:p.Ala658Asp
|
|
XM_011535018.2:c.1973C>A
|
XP_011533320.1:p.Ala658Asp
|
|
XM_017020486.1:c.2282C>A
|
XP_016875975.1:p.Ala761Asp
|
|
XM_017020487.1:c.1973C>A
|
XP_016875976.1:p.Ala658Asp
|
|
XM_017020488.1:c.1619C>A
|
XP_016875977.1:p.Ala540Asp
|
|
XM_017020489.1:c.1601C>A
|
XP_016875978.1:p.Ala534Asp
|
|
NM_004119.3:c.2498C>A
MANE Select
|
NP_004110.2:p.Ala833Asp
|
|
NR_130706.2:n.2696C>A
|
|
|