ENST00000333681.5:c.586-49892A>T
MANE Select
|
ENSP00000329623.3:n.586-49892A>T
|
|
ENST00000677227.1:c.914-49892A>T
|
ENSP00000504566.1:n.914-49892A>T
|
|
ENST00000678134.1:c.790-49892A>T
|
ENSP00000503628.1:n.790-49892A>T
|
|
ENST00000678349.1:c.1138-49892A>T
|
ENSP00000504190.1:n.1138-49892A>T
|
|
ENST00000333681.4:c.586-49892A>T
|
ENSP00000329623.3:n.586-49892A>T
|
|
ENST00000398117.1:c.586-49892A>T
|
ENSP00000381185.1:n.586-49892A>T
|
|
NM_000633.2:c.586-49892A>T
|
NP_000624.2:n.586-49892A>T
|
|
XR_935246.1:n.2026-49892A>T
|
|
|
XR_935248.1:n.1805-49892A>T
|
|
|
XR_935248.3:n.2307-49892A>T
|
|
|
NM_000633.3:c.586-49892A>T
MANE Select
|
NP_000624.2:n.586-49892A>T
|
|