|
ENST00000359128.10:c.2526A>G
MANE Select
|
ENSP00000352039.6:p.Arg842=
|
|
|
ENST00000324659.12:c.2667A>G
|
ENSP00000323897.9:p.Arg889=
|
|
|
ENST00000359128.9:c.2526A>G
|
ENSP00000352039.6:p.Arg842=
|
|
|
ENST00000448023.6:c.2526A>G
|
ENSP00000414415.3:p.Arg842=
|
|
|
ENST00000615877.4:c.*376A>G
|
ENSP00000482989.1:n.*376A>G
|
|
|
ENST00000618137.1:c.427A>G
|
|
|
|
NM_178844.3:c.2526A>G
|
NP_849172.2:p.Arg842=
|
|
|
NR_075083.2:n.3147A>G
|
|
|
|
XM_011522416.1:c.2526A>G
|
XP_011520718.1:p.Arg842=
|
|
|
XM_011522417.1:c.2526A>G
|
XP_011520719.1:p.Arg842=
|
|
|
XM_011522418.1:c.2526A>G
|
XP_011520720.1:p.Arg842=
|
|
|
XM_011522419.1:c.2526A>G
|
XP_011520721.1:p.Arg842=
|
|
|
XM_011522420.1:c.2526A>G
|
XP_011520722.1:p.Arg842=
|
|
|
XM_011522421.1:c.2526A>G
|
XP_011520723.1:p.Arg842=
|
|
|
XM_011522422.1:c.2526A>G
|
XP_011520724.1:p.Arg842=
|
|
|
XM_011522423.1:c.2526A>G
|
XP_011520725.1:p.Arg842=
|
|
|
XR_243342.2:n.501+3221T>C
|
|
|
|
XR_933023.1:n.501+3221T>C
|
|
|
|
XR_933024.1:n.466+3221T>C
|
|
|
|
XR_933025.1:n.411+3221T>C
|
|
|
|
XM_017023027.2:c.2553A>G
|
XP_016878516.1:p.Arg851=
|
|
|
XM_017023028.2:c.2553A>G
|
XP_016878517.1:p.Arg851=
|
|
|
XM_017023029.2:c.2553A>G
|
XP_016878518.1:p.Arg851=
|
|
|
XM_017023030.2:c.2553A>G
|
XP_016878519.1:p.Arg851=
|
|
|
XM_017023031.2:c.2553A>G
|
XP_016878520.1:p.Arg851=
|
|
|
XM_017023033.2:c.2553A>G
|
XP_016878522.1:p.Arg851=
|
|
|
XM_017023034.2:c.2553A>G
|
XP_016878523.1:p.Arg851=
|
|
|
XM_017023035.2:c.2553A>G
|
XP_016878524.1:p.Arg851=
|
|
|
XM_017023036.2:c.2553A>G
|
XP_016878525.1:p.Arg851=
|
|
|
XM_017023037.2:c.2448A>G
|
XP_016878526.1:p.Arg816=
|
|
|
XM_017023038.2:c.2421A>G
|
XP_016878527.1:p.Arg807=
|
|
|
XM_017023039.1:c.2553A>G
|
XP_016878528.1:p.Arg851=
|
|
|
XR_001752059.2:n.2497+3221T>C
|
|
|
|
XR_001752060.2:n.2497+3221T>C
|
|
|
|
NM_178844.4:c.2526A>G
MANE Select
|
NP_849172.2:p.Arg842=
|
|
|
NR_075083.3:n.3146A>G
|
|
|
