ENST00000256906.5:c.876T>G
MANE Select
|
ENSP00000256906.4:p.His292Gln
|
|
ENST00000256906.4:c.876T>G
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ENSP00000256906.4:p.His292Gln
|
|
ENST00000426880.2:c.612T>G
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ENSP00000402526.2:p.His204Gln
|
|
NM_001143828.1:c.612T>G
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NP_001137300.1:p.His204Gln
|
|
NM_001160166.1:c.*508T>G
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NP_001153638.1:n.*508T>G
|
|
NM_021624.3:c.876T>G
|
NP_067637.2:p.His292Gln
|
|
XM_011526133.1:c.357+8314T>G
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XP_011524435.1:n.357+8314T>G
|
|
NM_021624.4:c.876T>G
MANE Select
|
NP_067637.2:p.His292Gln
|
|
NM_001143828.2:c.612T>G
|
NP_001137300.1:p.His204Gln
|
|
NM_001160166.2:c.*508T>G
|
NP_001153638.1:n.*508T>G
|
|