ENST00000425340.3:c.592G>A
MANE Select
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ENSP00000387498.2:p.Val198Ile
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ENST00000522966.2:c.592G>A
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ENSP00000430227.2:p.Val198Ile
|
|
ENST00000391876.5:c.592G>A
|
ENSP00000375748.4:p.Val198Ile
|
|
ENST00000425340.2:c.592G>A
|
ENSP00000387498.2:p.Val198Ile
|
|
ENST00000522966.1:c.592G>A
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ENSP00000430227.1:p.Val198Ile
|
|
NM_000511.5:c.592G>A
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NP_000502.4:p.Val198Ile
|
|
NM_001097638.2:c.592G>A
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NP_001091107.1:p.Val198Ile
|
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NR_131188.1:n.301C>T
|
|
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NM_000511.6:c.592G>A
MANE Select
|
NP_000502.4:p.Val198Ile
|
|
NM_001097638.3:c.592G>A
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NP_001091107.1:p.Val198Ile
|
|