ENST00000332896.8:c.482T>G
MANE Select
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ENSP00000327647.3:p.Val161Gly
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ENST00000332896.7:c.482T>G
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ENSP00000327647.3:p.Val161Gly
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ENST00000542893.2:c.482T>G
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ENSP00000439068.2:p.Val161Gly
|
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ENST00000548330.1:n.867T>G
|
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ENST00000548483.5:c.299-43897T>G
|
ENSP00000448685.1:n.299-43897T>G
|
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ENST00000550030.1:n.282T>G
|
|
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ENST00000551065.5:c.299-9166T>G
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ENSP00000448425.1:n.299-9166T>G
|
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ENST00000609189.1:n.258T>G
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|
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NM_003805.3:c.482T>G
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NP_003796.1:p.Val161Gly
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XM_005269211.3:c.299-43897T>G
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XP_005269268.1:n.299-43897T>G
|
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NM_001320099.1:c.482T>G
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NP_001307028.1:p.Val161Gly
|
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NM_001320100.1:c.299-43897T>G
|
NP_001307029.1:n.299-43897T>G
|
|
NM_003805.4:c.482T>G
|
NP_003796.1:p.Val161Gly
|
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NR_135147.1:n.407-9166T>G
|
|
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XM_017020144.1:c.299-9166T>G
|
XP_016875633.1:n.299-9166T>G
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XR_001748910.1:n.430-9166T>G
|
|
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NM_003805.5:c.482T>G
MANE Select
|
NP_003796.1:p.Val161Gly
|
|
NM_001320099.2:c.482T>G
|
NP_001307028.1:p.Val161Gly
|
|
NM_001320100.2:c.299-43897T>G
|
NP_001307029.1:n.299-43897T>G
|
|
NR_135147.2:n.403-9166T>G
|
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