ENST00000413272.7:c.712-1292C=
MANE Select
|
ENSP00000408697.2:n.712-1292C=
|
|
ENST00000413272.6:c.712-1292C=
|
ENSP00000408697.2:n.712-1292C=
|
|
NM_001010906.1:c.712-1292C=
|
NP_001010906.1:n.712-1292C=
|
|
XM_011544523.1:c.784-1292C=
|
XP_011542825.1:n.784-1292C=
|
|
XM_011544524.1:c.784-1292C=
|
XP_011542826.1:n.784-1292C=
|
|
XM_011544526.1:c.784-1292C=
|
XP_011542828.1:n.784-1292C=
|
|
XM_011544523.2:c.784-1292C=
|
XP_011542825.1:n.784-1292C=
|
|
XM_011544524.3:c.784-1292C=
|
XP_011542826.1:n.784-1292C=
|
|
XM_011544526.2:c.784-1292C=
|
XP_011542828.1:n.784-1292C=
|
|
XM_017013403.1:c.784-1292C=
|
XP_016868892.1:n.784-1292C=
|
|
NM_001010906.2:c.712-1292C=
MANE Select
|
NP_001010906.1:n.712-1292C=
|
|