NM_032444.4:c.3467A>C
MANE Select
|
NP_115820.2:p.Asp1156Ala
|
ENST00000294008.4:c.3467A>C
MANE Select
|
ENSP00000294008.3:p.Asp1156Ala
|
NM_032444.2:c.3467A>C , LRG_503t1:c.3467A>C
|
NP_115820.2:p.Asp1156Ala
|
NM_032444.3:c.3467A>C
|
NP_115820.2:p.Asp1156Ala
|
ENST00000294008.3:c.3467A>C
|
ENSP00000294008.3:p.Asp1156Ala
|
XM_011522715.1:c.3467A>C
|
XP_011521017.1:p.Asp1156Ala
|
XM_011522715.3:c.3467A>C
|
XP_011521017.1:p.Asp1156Ala
|
XM_017023775.2:c.2645A>C
|
XP_016879264.1:p.Asp882Ala
|
XM_024450471.1:c.3467A>C
|
XP_024306239.1:p.Asp1156Ala
|