ENST00000463045.3:c.-18G=
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ENSP00000481376.2:n.-18G=
|
|
ENST00000491274.6:c.112G=
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ENSP00000480482.2:p.Ala38=
|
|
ENST00000375499.8:c.154G=
MANE Select
|
ENSP00000364649.3:p.Ala52=
|
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ENST00000375499.7:c.154G=
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ENSP00000364649.3:p.Ala52=
|
|
ENST00000463045.2:c.-18G=
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ENSP00000481376.1:n.-18G=
|
|
ENST00000466613.2:n.166G=
|
|
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ENST00000475506.1:n.71G=
|
|
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ENST00000485515.5:n.142G=
|
|
|
ENST00000491274.5:c.112G=
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ENSP00000480482.1:p.Ala38=
|
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NM_003000.2:c.154G= , LRG_316t1:c.154G=
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NP_002991.2:p.Ala52=
|
|
NM_003000.3:c.154G=
MANE Select
|
NP_002991.2:p.Ala52=
|
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