ENST00000394975.3:c.383T>G
MANE Select
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ENSP00000378426.2:p.Leu128Arg
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ENST00000300851.10:c.444T>G
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ENSP00000300851.6:p.Ala148=
|
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ENST00000319788.11:c.465T>G
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ENSP00000326135.7:p.Ala155=
|
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ENST00000354895.4:c.273T>G
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ENSP00000346969.4:p.Ala91=
|
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ENST00000394971.7:c.477T>G
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ENSP00000378422.3:p.Ala159=
|
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ENST00000394975.2:c.383T>G
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ENSP00000378426.2:p.Leu128Arg
|
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ENST00000420057.2:c.345T>G
|
|
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ENST00000472468.1:c.68T>G
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ENSP00000458994.1:p.Leu23Arg
|
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ENST00000498155.1:c.480T>G
|
ENSP00000417662.1:p.Ala160=
|
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ENST00000529564.1:c.283+2069T>G
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ENSP00000431371.1:n.283+2069T>G
|
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ENST00000532364.1:c.173+3314T>G
|
ENSP00000460316.1:n.173+3314T>G
|
|
ENST00000533518.5:c.256T>G
|
|
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NM_001311311.1:c.467T>G
|
NP_001298240.1:p.Leu156Arg
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|
NM_024006.4:c.383T>G
|
NP_076869.1:p.Leu128Arg
|
|
NM_024006.5:c.383T>G
|
NP_076869.1:p.Leu128Arg
|
|
NM_206824.1:c.273T>G
|
NP_996560.1:p.Ala91=
|
|
NM_206824.2:c.273T>G
|
NP_996560.1:p.Ala91=
|
|
XM_011545944.1:c.383T>G
|
XP_011544246.1:p.Leu128Arg
|
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XM_011545945.1:c.273T>G
|
XP_011544247.1:p.Ala91=
|
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XR_950848.1:n.1171T>G
|
|
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NM_024006.6:c.383T>G
MANE Select
|
NP_076869.1:p.Leu128Arg
|
|
NM_001311311.2:c.467T>G
|
NP_001298240.1:p.Leu156Arg
|
|
NM_206824.3:c.273T>G
|
NP_996560.1:p.Ala91=
|
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