ENST00000233627.14:c.442G>A
MANE Select
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ENSP00000233627.9:p.Val148Ile
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ENST00000233627.13:c.442G>A
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ENSP00000233627.9:p.Val148Ile
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ENST00000313408.11:c.442G>A
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ENSP00000364262.5:p.Val148Ile
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ENST00000414651.3:c.532G>A
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ENSP00000406630.2:p.Val178Ile
|
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ENST00000436115.6:n.2397G>A
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ENST00000534853.5:c.*236G>A
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ENSP00000442822.1:n.*236G>A
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ENST00000535382.1:n.694G>A
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|
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ENST00000538523.5:n.498G>A
|
|
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ENST00000538662.5:n.537G>A
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|
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ENST00000538929.5:n.532G>A
|
|
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ENST00000539480.5:c.442G>A
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ENSP00000443273.1:p.Val148Ile
|
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ENST00000540530.5:n.433G>A
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|
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ENST00000543289.5:n.1000G>A
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|
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ENST00000545446.5:n.733G>A
|
|
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ENST00000546172.7:c.*438G>A
|
ENSP00000467094.1:n.*438G>A
|
|
ENST00000546283.5:c.442G>A
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ENSP00000440348.1:p.Val148Ile
|
|
ENST00000618074.4:c.449G>A
|
ENSP00000477895.1:p.Gly150Asp
|
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ENST00000620479.4:c.446G>A
|
ENSP00000480984.1:p.Gly149Asp
|
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ENST00000622587.4:n.506G>A
|
|
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NM_024407.4:c.442G>A
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NP_077718.3:p.Val148Ile
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XM_005259556.3:c.442G>A
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XP_005259613.2:p.Val148Ile
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NM_001363602.1:c.442G>A
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NP_001350531.1:p.Val148Ile
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XM_024451499.1:c.463G>A
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XP_024307267.1:p.Val155Ile
|
|
NM_024407.5:c.442G>A
MANE Select
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NP_077718.3:p.Val148Ile
|
|
NM_001363602.2:c.442G>A
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NP_001350531.1:p.Val148Ile
|
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