ENST00000295897.9:c.511C>G
MANE Select
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ENSP00000295897.4:p.Pro171Ala
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ENST00000295897.8:c.511C>G
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ENSP00000295897.4:p.Pro171Ala
|
|
ENST00000401494.7:c.166C>G
|
ENSP00000384695.3:p.Pro56Ala
|
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ENST00000415165.6:c.138-2613C>G
|
ENSP00000401820.2:n.138-2613C>G
|
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ENST00000441319.5:c.517C>G
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ENSP00000392541.1:p.Pro173Ala
|
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ENST00000476441.6:c.108C>G
|
ENSP00000423727.1:p.Ile36Met
|
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ENST00000503124.5:c.61C>G
|
ENSP00000421027.1:p.Pro21Ala
|
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ENST00000505649.5:n.197C>G
|
|
|
ENST00000509063.5:c.511C>G
|
ENSP00000422784.1:p.Pro171Ala
|
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ENST00000511370.1:c.44C>G
|
|
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ENST00000514786.1:n.480C>G
|
|
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ENST00000621085.4:c.490+21C>G
|
ENSP00000483421.1:n.490+21C>G
|
|
ENST00000621628.4:c.486+307C>G
|
ENSP00000480485.1:n.486+307C>G
|
|
NM_000477.5:c.511C>G
|
NP_000468.1:p.Pro171Ala
|
|
NM_000477.6:c.511C>G
|
NP_000468.1:p.Pro171Ala
|
|
NM_000477.7:c.511C>G
MANE Select
|
NP_000468.1:p.Pro171Ala
|
|