ENST00000281928.9:c.5891-69C>G
MANE Select
|
ENSP00000281928.3:n.5891-69C>G
|
|
ENST00000548694.2:n.881-69C>G
|
|
|
ENST00000548784.2:n.2105-69C>G
|
|
|
ENST00000648379.1:n.4259-69C>G
|
|
|
ENST00000648737.1:n.5655-69C>G
|
|
|
ENST00000648825.1:n.4076-69C>G
|
|
|
ENST00000648916.1:n.3902-69C>G
|
|
|
ENST00000649607.1:c.4075-69C>G
|
|
|
ENST00000649775.1:c.2380-69C>G
|
|
|
ENST00000650226.1:c.5927-69C>G
|
ENSP00000496981.1:n.5927-69C>G
|
|
ENST00000281928.7:c.5891-69C>G
|
ENSP00000281928.3:n.5891-69C>G
|
|
ENST00000548784.1:n.389-69C>G
|
|
|
ENST00000552447.1:c.504-69C>G
|
|
|
NM_015335.4:c.5891-69C>G
|
NP_056150.1:n.5891-69C>G
|
|
XM_011538080.1:c.5927-69C>G
|
XP_011536382.1:n.5927-69C>G
|
|
XM_011538081.1:c.5924-69C>G
|
XP_011536383.1:n.5924-69C>G
|
|
XM_011538082.1:c.5897-69C>G
|
XP_011536384.1:n.5897-69C>G
|
|
XM_011538080.2:c.5927-69C>G
|
XP_011536382.1:n.5927-69C>G
|
|
XM_011538081.2:c.5924-69C>G
|
XP_011536383.1:n.5924-69C>G
|
|
XM_011538082.2:c.5897-69C>G
|
XP_011536384.1:n.5897-69C>G
|
|
XM_017019090.1:c.5888-69C>G
|
XP_016874579.1:n.5888-69C>G
|
|
NM_015335.5:c.5891-69C>G
MANE Select
|
NP_056150.1:n.5891-69C>G
|
|