ENST00000295897.9:c.1168C>G
MANE Select
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ENSP00000295897.4:p.Pro390Ala
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ENST00000295897.8:c.1168C>G
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ENSP00000295897.4:p.Pro390Ala
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ENST00000401494.7:c.823C>G
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ENSP00000384695.3:p.Pro275Ala
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ENST00000415165.6:c.592C>G
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ENSP00000401820.2:p.Pro198Ala
|
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ENST00000476441.6:c.*447C>G
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ENSP00000423727.1:n.*447C>G
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ENST00000484992.1:n.488C>G
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|
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ENST00000503124.5:c.718C>G
|
ENSP00000421027.1:p.Pro240Ala
|
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ENST00000504043.1:n.171C>G
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|
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ENST00000505649.5:n.854C>G
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|
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ENST00000509063.5:c.1168C>G
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ENSP00000422784.1:p.Pro390Ala
|
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ENST00000511370.1:c.701C>G
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|
|
ENST00000621085.4:c.529C>G
|
ENSP00000483421.1:p.Pro177Ala
|
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ENST00000621628.4:c.529C>G
|
ENSP00000480485.1:p.Pro177Ala
|
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NM_000477.5:c.1168C>G
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NP_000468.1:p.Pro390Ala
|
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NM_000477.6:c.1168C>G
|
NP_000468.1:p.Pro390Ala
|
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NM_000477.7:c.1168C>G
MANE Select
|
NP_000468.1:p.Pro390Ala
|
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