ENST00000446632.7:c.995-369G=
MANE Select
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ENSP00000412209.2:n.995-369G=
|
|
ENST00000256452.7:c.995-369G=
|
ENSP00000256452.3:n.995-369G=
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|
ENST00000418488.6:c.710-369G=
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ENSP00000388858.2:n.710-369G=
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|
ENST00000438560.5:c.995-369G=
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ENSP00000390753.1:n.995-369G=
|
|
ENST00000446632.6:c.995-369G=
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ENSP00000412209.2:n.995-369G=
|
|
NM_000564.4:c.995-369G=
|
NP_000555.2:n.995-369G=
|
|
NM_001243099.1:c.995-369G=
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NP_001230028.1:n.995-369G=
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|
NM_175726.3:c.995-369G=
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NP_783853.1:n.995-369G=
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|
XM_011533677.1:c.995-369G=
|
XP_011531979.1:n.995-369G=
|
|
XM_011533678.1:c.995-369G=
|
XP_011531980.1:n.995-369G=
|
|
XM_011533677.2:c.995-369G=
|
XP_011531979.1:n.995-369G=
|
|
XM_011533678.2:c.995-369G=
|
XP_011531980.1:n.995-369G=
|
|
NM_000564.5:c.995-369G=
|
NP_000555.2:n.995-369G=
|
|
NM_001243099.2:c.995-369G=
|
NP_001230028.1:n.995-369G=
|
|
NM_175726.4:c.995-369G=
MANE Select
|
NP_783853.1:n.995-369G=
|
|