|
NM_032444.4:c.4740-6C>T
MANE Select
|
NP_115820.2:n.4740-6C>T
|
|
ENST00000294008.4:c.4740-6C>T
MANE Select
|
ENSP00000294008.3:n.4740-6C>T
|
|
NM_032444.2:c.4740-6C>T , LRG_503t1:c.4740-6C>T
|
NP_115820.2:n.4740-6C>T
|
|
NM_032444.3:c.4740-6C>T
|
NP_115820.2:n.4740-6C>T
|
|
ENST00000294008.3:c.4740-6C>T
|
ENSP00000294008.3:n.4740-6C>T
|
|
XM_011522715.1:c.4737-6C>T
|
XP_011521017.1:n.4737-6C>T
|
|
XM_011522715.3:c.4737-6C>T
|
XP_011521017.1:n.4737-6C>T
|
|
XM_017023775.2:c.3918-6C>T
|
XP_016879264.1:n.3918-6C>T
|
|
XM_024450471.1:c.4740-6C>T
|
XP_024306239.1:n.4740-6C>T
|