|
NM_006947.4:c.826-39T=
MANE Select
|
NP_008878.3:n.826-39T=
|
|
ENST00000642900.1:c.826-39T=
MANE Select
|
ENSP00000495128.1:n.826-39T=
|
|
NM_001267722.1:c.643-39T=
|
NP_001254651.1:n.643-39T=
|
|
NM_001267722.2:c.643-39T=
|
NP_001254651.1:n.643-39T=
|
|
NM_006947.3:c.826-39T=
|
NP_008878.3:n.826-39T=
|
|
NR_151856.1:n.866-39T=
|
|
|
NR_151856.2:n.845-39T=
|
|
|
ENST00000342756.9:c.826-39T=
|
ENSP00000342181.5:n.826-39T=
|
|
ENST00000505314.1:c.392-1636T=
|
|
|
ENST00000505314.2:c.726-1636T=
|
|
|
ENST00000510663.5:c.643-39T=
|
ENSP00000424576.1:n.643-39T=
|
|
ENST00000510663.6:c.643-39T=
|
ENSP00000424576.1:n.643-39T=
|
|
XM_005265765.3:c.826-39T=
|
XP_005265822.2:n.826-39T=
|
|
XM_024454192.1:c.826-39T=
|
XP_024309960.1:n.826-39T=
|