ENST00000622290.5:c.2965G>C
|
ENSP00000483331.2:p.Gly989Arg
|
|
ENST00000205557.12:c.2965G>C
MANE Select
|
ENSP00000205557.7:p.Gly989Arg
|
|
ENST00000205557.11:c.2965G>C
|
ENSP00000205557.7:p.Gly989Arg
|
|
ENST00000456970.6:c.2790G>C
|
ENSP00000405002.2:n.2790G>C
|
|
ENST00000622290.4:c.*174G>C
|
ENSP00000483331.1:n.*174G>C
|
|
NM_001171.5:c.2965G>C
|
NP_001162.4:p.Gly989Arg
|
|
XM_011522479.1:c.2932G>C
|
XP_011520781.1:p.Gly978Arg
|
|
XM_011522480.1:c.2623G>C
|
XP_011520782.1:p.Gly875Arg
|
|
XM_011522481.1:c.2623G>C
|
XP_011520783.1:p.Gly875Arg
|
|
XR_932836.1:n.3200G>C
|
|
|
XR_932837.1:n.3201G>C
|
|
|
XR_932838.1:n.3201G>C
|
|
|
NM_001351800.1:c.2623G>C
|
NP_001338729.1:p.Gly875Arg
|
|
NR_147784.1:n.2827G>C
|
|
|
XM_011522479.2:c.2932G>C
|
XP_011520781.1:p.Gly978Arg
|
|
XM_011522481.3:c.2623G>C
|
XP_011520783.1:p.Gly875Arg
|
|
XM_017023212.1:c.2797G>C
|
XP_016878701.1:p.Gly933Arg
|
|
XM_017023214.1:c.2965G>C
|
XP_016878703.1:p.Gly989Arg
|
|
XM_024450261.1:c.3001G>C
|
XP_024306029.1:p.Gly1001Arg
|
|
XR_932836.2:n.3146G>C
|
|
|
XR_932837.3:n.3146G>C
|
|
|
XR_932838.3:n.3146G>C
|
|
|
NM_001171.6:c.2965G>C
MANE Select
|
NP_001162.5:p.Gly989Arg
|
|