ENST00000221930.6:c.861-194G>T
MANE Select
|
ENSP00000221930.4:n.861-194G>T
|
|
ENST00000600196.2:c.713-194G>T
|
ENSP00000504008.1:n.713-194G>T
|
|
ENST00000677934.1:c.635-194G>T
|
ENSP00000504769.1:n.635-194G>T
|
|
ENST00000221930.5:c.861-194G>T
|
ENSP00000221930.4:n.861-194G>T
|
|
ENST00000598758.5:c.149-194G>T
|
|
|
ENST00000600196.1:n.173-194G>T
|
|
|
NM_000660.5:c.861-194G>T
|
NP_000651.3:n.861-194G>T
|
|
XM_011527242.1:c.864-194G>T
|
XP_011525544.1:n.864-194G>T
|
|
NM_000660.6:c.861-194G>T
|
NP_000651.3:n.861-194G>T
|
|
XM_011527242.2:c.864-194G>T
|
XP_011525544.1:n.864-194G>T
|
|
NM_000660.7:c.861-194G>T
MANE Select
|
NP_000651.3:n.861-194G>T
|
|