ENST00000394975.3:c.381G>T
MANE Select
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ENSP00000378426.2:p.Val127=
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ENST00000300851.10:c.442G>T
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ENSP00000300851.6:p.Ala148Ser
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ENST00000319788.11:c.463G>T
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ENSP00000326135.7:p.Ala155Ser
|
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ENST00000354895.4:c.271G>T
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ENSP00000346969.4:p.Ala91Ser
|
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ENST00000394971.7:c.475G>T
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ENSP00000378422.3:p.Ala159Ser
|
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ENST00000394975.2:c.381G>T
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ENSP00000378426.2:p.Val127=
|
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ENST00000420057.2:c.343G>T
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|
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ENST00000472468.1:c.66G>T
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ENSP00000458994.1:p.Val22=
|
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ENST00000498155.1:c.478G>T
|
ENSP00000417662.1:p.Ala160Ser
|
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ENST00000529564.1:c.283+2067G>T
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ENSP00000431371.1:n.283+2067G>T
|
|
ENST00000532364.1:c.173+3312G>T
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ENSP00000460316.1:n.173+3312G>T
|
|
ENST00000533518.5:c.254G>T
|
|
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NM_001311311.1:c.465G>T
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NP_001298240.1:p.Val155=
|
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NM_024006.4:c.381G>T
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NP_076869.1:p.Val127=
|
|
NM_024006.5:c.381G>T
|
NP_076869.1:p.Val127=
|
|
NM_206824.1:c.271G>T
|
NP_996560.1:p.Ala91Ser
|
|
NM_206824.2:c.271G>T
|
NP_996560.1:p.Ala91Ser
|
|
XM_011545944.1:c.381G>T
|
XP_011544246.1:p.Val127=
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|
XM_011545945.1:c.271G>T
|
XP_011544247.1:p.Ala91Ser
|
|
XR_950848.1:n.1169G>T
|
|
|
NM_024006.6:c.381G>T
MANE Select
|
NP_076869.1:p.Val127=
|
|
NM_001311311.2:c.465G>T
|
NP_001298240.1:p.Val155=
|
|
NM_206824.3:c.271G>T
|
NP_996560.1:p.Ala91Ser
|
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