ENST00000615310.5:c.2279A>C
|
ENSP00000480088.2:p.Asp760Ala
|
|
ENST00000683007.1:n.2249A>C
|
|
|
ENST00000683872.1:n.2240A>C
|
|
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ENST00000340058.6:c.2675A>C
|
ENSP00000344798.4:p.Asp892Ala
|
|
ENST00000355710.8:c.2675A>C
MANE Select
|
ENSP00000347942.3:p.Asp892Ala
|
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ENST00000671844.1:c.*1269A>C
|
ENSP00000500541.1:n.*1269A>C
|
|
ENST00000672389.1:c.*1269A>C
|
ENSP00000500252.1:n.*1269A>C
|
|
ENST00000340058.5:c.2675A>C
|
ENSP00000344798.4:p.Asp892Ala
|
|
ENST00000355710.7:c.2675A>C
|
ENSP00000347942.3:p.Asp892Ala
|
|
ENST00000615310.4:c.*24A>C
|
ENSP00000480088.1:n.*24A>C
|
|
NM_020630.4:c.2675A>C , LRG_518t2:c.2675A>C
|
NP_065681.1:p.Asp892Ala
|
|
NM_020975.4:c.2675A>C , LRG_518t1:c.2675A>C
|
NP_066124.1:p.Asp892Ala
|
|
XM_011540027.1:c.2675A>C
|
XP_011538329.1:p.Asp892Ala
|
|
NM_001355216.1:c.1913A>C
|
NP_001342145.1:p.Asp638Ala
|
|
NM_020630.5:c.2675A>C
|
NP_065681.1:p.Asp892Ala
|
|
NM_020975.5:c.2675A>C
|
NP_066124.1:p.Asp892Ala
|
|
NM_020975.6:c.2675A>C
MANE Select
|
NP_066124.1:p.Asp892Ala
|
|
NM_020630.6:c.2675A>C
|
NP_065681.1:p.Asp892Ala
|
|