ENST00000265080.9:c.1838+1669A>G
MANE Select
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ENSP00000265080.4:n.1838+1669A>G
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|
ENST00000265080.8:c.1838+1669A>G
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ENSP00000265080.4:n.1838+1669A>G
|
|
ENST00000503795.1:c.1838+1669A>G
|
ENSP00000421771.1:n.1838+1669A>G
|
|
NM_006909.2:c.1838+1669A>G
|
NP_008840.1:n.1838+1669A>G
|
|
XM_005248565.1:c.1838+1669A>G
|
XP_005248622.1:n.1838+1669A>G
|
|
XM_017009682.2:c.1553+1669A>G
|
XP_016865171.1:n.1553+1669A>G
|
|
XM_017009683.1:c.1838+1669A>G
|
XP_016865172.1:n.1838+1669A>G
|
|
XM_024446141.1:c.1838+1669A>G
|
XP_024301909.1:n.1838+1669A>G
|
|
XR_002956166.1:n.1905+1669A>G
|
|
|
NM_006909.3:c.1838+1669A>G
MANE Select
|
NP_008840.1:n.1838+1669A>G
|
|