|
NM_032444.4:c.1115G>A
MANE Select
|
NP_115820.2:p.Arg372Gln
|
|
ENST00000294008.4:c.1115G>A
MANE Select
|
ENSP00000294008.3:p.Arg372Gln
|
|
NM_032444.2:c.1115G>A , LRG_503t1:c.1115G>A
|
NP_115820.2:p.Arg372Gln
|
|
NM_032444.3:c.1115G>A
|
NP_115820.2:p.Arg372Gln
|
|
ENST00000294008.3:c.1115G>A
|
ENSP00000294008.3:p.Arg372Gln
|
|
ENST00000466154.5:n.2336G>A
|
|
|
ENST00000486524.1:n.2669G>A
|
|
|
ENST00000697858.1:n.456G>A
|
|
|
XM_011522715.1:c.1115G>A
|
XP_011521017.1:p.Arg372Gln
|
|
XM_011522715.3:c.1115G>A
|
XP_011521017.1:p.Arg372Gln
|
|
XM_017023775.2:c.-813G>A
|
XP_016879264.1:n.-813G>A
|
|
XM_024450471.1:c.1115G>A
|
XP_024306239.1:p.Arg372Gln
|