ENST00000333681.5:c.585+12869A>G
MANE Select
|
ENSP00000329623.3:n.585+12869A>G
|
|
ENST00000677227.1:c.585+12869A>G
|
ENSP00000504566.1:n.585+12869A>G
|
|
ENST00000678134.1:c.586-3348A>G
|
ENSP00000503628.1:n.586-3348A>G
|
|
ENST00000678349.1:c.1137+12317A>G
|
ENSP00000504190.1:n.1137+12317A>G
|
|
ENST00000333681.4:c.585+12869A>G
|
ENSP00000329623.3:n.585+12869A>G
|
|
ENST00000398117.1:c.585+12869A>G
|
ENSP00000381185.1:n.585+12869A>G
|
|
NM_000633.2:c.585+12869A>G
|
NP_000624.2:n.585+12869A>G
|
|
XM_011526135.1:c.586-2366A>G
|
XP_011524437.1:n.586-2366A>G
|
|
XR_935246.1:n.1697+12869A>G
|
|
|
XR_935247.1:n.1697+12869A>G
|
|
|
XR_935248.1:n.1476+12869A>G
|
|
|
XM_011526135.3:c.586-2366A>G
|
XP_011524437.1:n.586-2366A>G
|
|
XM_017025917.2:c.586-3348A>G
|
XP_016881406.1:n.586-3348A>G
|
|
XR_935248.3:n.1978+12869A>G
|
|
|
NM_000633.3:c.585+12869A>G
MANE Select
|
NP_000624.2:n.585+12869A>G
|
|