ENST00000225964.10:c.858+31C>G
MANE Select
|
ENSP00000225964.6:n.858+31C>G
|
|
ENST00000225964.9:c.858+31C>G
|
ENSP00000225964.5:n.858+31C>G
|
|
ENST00000485870.1:n.10C>G
|
|
|
ENST00000495677.1:n.585+31C>G
|
|
|
NM_000088.3:c.858+31C>G , LRG_1t1:c.858+31C>G
|
NP_000079.2:n.858+31C>G
|
|
XM_005257058.3:c.858+31C>G
|
XP_005257115.2:n.858+31C>G
|
|
XM_005257059.3:c.858+31C>G
|
XP_005257116.2:n.858+31C>G
|
|
XM_011524341.1:c.858+31C>G
|
XP_011522643.1:n.858+31C>G
|
|
XM_005257058.4:c.858+31C>G
|
XP_005257115.2:n.858+31C>G
|
|
XM_005257059.4:c.858+31C>G
|
XP_005257116.2:n.858+31C>G
|
|
NM_000088.4:c.858+31C>G
MANE Select
|
NP_000079.2:n.858+31C>G
|
|