ENST00000298139.7:c.4234G>T
MANE Select
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ENSP00000298139.5:p.Ala1412Ser
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ENST00000650667.1:c.*3848G>T
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ENSP00000498593.1:n.*3848G>T
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ENST00000651946.1:n.458G>T
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ENST00000298139.5:c.4234G>T
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ENSP00000298139.5:p.Ala1412Ser
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ENST00000521620.5:n.2867G>T
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NM_000553.4:c.4234G>T , LRG_524t1:c.4234G>T
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NP_000544.2:p.Ala1412Ser
|
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XM_011544639.1:c.4153G>T
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XP_011542941.1:p.Ala1385Ser
|
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XM_011544640.1:c.2635G>T
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XP_011542942.1:p.Ala879Ser
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XR_949643.1:n.88-1719C>A
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XR_949644.1:n.88-1719C>A
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XR_949645.1:n.88-1719C>A
|
|
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XR_949646.1:n.88-1719C>A
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|
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XR_949647.1:n.701-1719C>A
|
|
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XR_949648.1:n.603-1719C>A
|
|
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NM_000553.5:c.4234G>T
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NP_000544.2:p.Ala1412Ser
|
|
XM_011544639.3:c.4153G>T
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XP_011542941.1:p.Ala1385Ser
|
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XM_024447265.1:c.4024G>T
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XP_024303033.1:p.Ala1342Ser
|
|
NM_000553.6:c.4234G>T
MANE Select
|
NP_000544.2:p.Ala1412Ser
|
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