ENST00000333681.5:c.586-24628C>T
MANE Select
|
ENSP00000329623.3:n.586-24628C>T
|
|
ENST00000677227.1:c.914-24628C>T
|
ENSP00000504566.1:n.914-24628C>T
|
|
ENST00000678134.1:c.790-24628C>T
|
ENSP00000503628.1:n.790-24628C>T
|
|
ENST00000678301.1:c.24+4686C>T
|
ENSP00000504546.1:n.24+4686C>T
|
|
ENST00000678349.1:c.1138-24628C>T
|
ENSP00000504190.1:n.1138-24628C>T
|
|
ENST00000333681.4:c.586-24628C>T
|
ENSP00000329623.3:n.586-24628C>T
|
|
ENST00000398117.1:c.586-24628C>T
|
ENSP00000381185.1:n.586-24628C>T
|
|
ENST00000590515.1:n.24+8459C>T
|
|
|
NM_000633.2:c.586-24628C>T
|
NP_000624.2:n.586-24628C>T
|
|
XR_935246.1:n.2026-24628C>T
|
|
|
XR_935248.1:n.1805-24628C>T
|
|
|
XR_935248.3:n.2307-24628C>T
|
|
|
NM_000633.3:c.586-24628C>T
MANE Select
|
NP_000624.2:n.586-24628C>T
|
|