ENST00000261978.9:c.4721-39G>A
MANE Select
|
ENSP00000261978.4:n.4721-39G>A
|
|
ENST00000261978.8:c.4721-39G>A
|
ENSP00000261978.4:n.4721-39G>A
|
|
ENST00000553939.5:c.4721-39G>A
|
ENSP00000452110.1:n.4721-39G>A
|
|
ENST00000556690.5:c.4589-39G>A
|
ENSP00000451477.1:n.4589-39G>A
|
|
NM_000428.2:c.4721-39G>A
|
NP_000419.1:n.4721-39G>A
|
|
XM_011536765.1:c.4340-39G>A
|
XP_011535067.1:n.4340-39G>A
|
|
XM_011536766.1:c.4262-39G>A
|
XP_011535068.1:n.4262-39G>A
|
|
XM_011536767.1:c.4238-39G>A
|
XP_011535069.1:n.4238-39G>A
|
|
XM_011536765.2:c.4340-39G>A
|
XP_011535067.1:n.4340-39G>A
|
|
NM_000428.3:c.4721-39G>A
MANE Select
|
NP_000419.1:n.4721-39G>A
|
|