ENST00000324041.6:c.484C>G
MANE Select
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ENSP00000326159.1:p.Pro162Ala
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ENST00000324041.5:c.484C>G
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ENSP00000326159.1:p.Pro162Ala
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|
ENST00000431178.2:c.328+92C>G
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ENSP00000399448.2:n.328+92C>G
|
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ENST00000593885.1:c.195C>G
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ENSP00000469769.1:p.Cys65Trp
|
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ENST00000596876.1:n.486C>G
|
|
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ENST00000598305.5:c.195C>G
|
ENSP00000469963.1:p.Cys65Trp
|
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ENST00000599865.5:n.420C>G
|
|
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ENST00000602148.1:c.496C>G
|
ENSP00000472091.1:n.496C>G
|
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NM_001302961.1:c.199C>G
|
NP_001289890.1:p.Pro67Ala
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NM_004917.4:c.484C>G
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NP_004908.4:p.Pro162Ala
|
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NR_126566.1:n.473C>G
|
|
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XM_005259441.3:c.199C>G
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XP_005259498.2:p.Pro67Ala
|
|
XM_011527545.1:c.480C>G
|
XP_011525847.1:p.Cys160Trp
|
|
XM_011527546.1:c.475+92C>G
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XP_011525848.1:n.475+92C>G
|
|
XM_011527547.1:c.337C>G
|
XP_011525849.1:p.Pro113Ala
|
|
XM_005259441.4:c.199C>G
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XP_005259498.2:p.Pro67Ala
|
|
XM_011527545.3:c.480C>G
|
XP_011525847.1:p.Cys160Trp
|
|
XM_011527546.2:c.475+92C>G
|
XP_011525848.1:n.475+92C>G
|
|
NM_001302961.2:c.199C>G
|
NP_001289890.1:p.Pro67Ala
|
|
NR_126566.2:n.473C>G
|
|
|
NM_004917.5:c.484C>G
MANE Select
|
NP_004908.4:p.Pro162Ala
|
|