ENST00000320580.9:c.2656+316A>G
MANE Select
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ENSP00000316454.4:n.2656+316A>G
|
|
ENST00000320580.8:c.2656+316A>G
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ENSP00000316454.4:n.2656+316A>G
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|
ENST00000524815.5:c.40+316A>G
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ENSP00000433991.1:n.40+316A>G
|
|
ENST00000529677.1:c.206+316A>G
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|
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ENST00000529757.5:c.1264+316A>G
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ENSP00000432858.1:n.1264+316A>G
|
|
ENST00000531597.1:c.40+316A>G
|
ENSP00000434012.1:n.40+316A>G
|
|
NM_018026.3:c.2656+316A>G
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NP_060496.2:n.2656+316A>G
|
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XM_011545162.1:c.2335+316A>G
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XP_011543464.1:n.2335+316A>G
|
|
XM_011545163.1:c.2326+316A>G
|
XP_011543465.1:n.2326+316A>G
|
|
XM_011545164.1:c.2317+316A>G
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XP_011543466.1:n.2317+316A>G
|
|
XM_011545164.2:c.2317+316A>G
|
XP_011543466.1:n.2317+316A>G
|
|
NM_018026.4:c.2656+316A>G
MANE Select
|
NP_060496.2:n.2656+316A>G
|
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