ENST00000264381.8:c.1626A=
MANE Select
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ENSP00000264381.3:p.Leu542=
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|
ENST00000264381.7:c.1626A=
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ENSP00000264381.3:p.Leu542=
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|
ENST00000479451.5:c.216A=
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ENSP00000418325.1:p.Leu72=
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ENST00000482958.1:c.*132A=
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ENSP00000419804.1:n.*132A=
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|
ENST00000488954.1:c.216A=
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ENSP00000418504.1:p.Leu72=
|
|
ENST00000497011.5:c.1626A=
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ENSP00000419505.1:p.Leu542=
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|
NM_000055.2:c.1626A=
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NP_000046.1:p.Leu542=
|
|
XM_005247685.1:c.1749A=
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XP_005247742.1:p.Leu583=
|
|
NM_000055.3:c.1626A=
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NP_000046.1:p.Leu542=
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|
NR_137635.1:n.268A=
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|
|
NR_137636.1:n.1793A=
|
|
|
NM_000055.4:c.1626A=
MANE Select
|
NP_000046.1:p.Leu542=
|
|
NR_137635.2:n.219A=
|
|
|
NR_137636.2:n.1744A=
|
|
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