ENST00000302068.9:c.1093G>T
MANE Select
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ENSP00000306099.4:p.Ala365Ser
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ENST00000302068.8:c.1093G>T
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ENSP00000306099.4:p.Ala365Ser
|
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ENST00000502545.5:n.939+341G>T
|
|
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ENST00000509493.1:c.436G>T
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ENSP00000426757.1:p.Ala146Ser
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NM_001184741.1:c.916G>T
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NP_001171670.1:p.Ala306Ser
|
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NM_005141.4:c.1093G>T , LRG_558t1:c.1093G>T
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NP_005132.2:p.Ala365Ser
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NM_001382759.1:c.961G>T
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NP_001369688.1:p.Ala321Ser
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NM_001382760.1:c.1093G>T
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NP_001369689.1:p.Ala365Ser
|
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NM_001382761.1:c.1093G>T
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NP_001369690.1:p.Ala365Ser
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NM_001382762.1:c.793G>T
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NP_001369691.1:p.Ala265Ser
|
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NM_001382763.1:c.1084G>T
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NP_001369692.1:p.Ala362Ser
|
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NM_001382764.1:c.1080+13G>T
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NP_001369693.1:n.1080+13G>T
|
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NM_001382765.1:c.1093G>T
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NP_001369694.1:p.Ala365Ser
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NM_005141.5:c.1093G>T
MANE Select
|
NP_005132.2:p.Ala365Ser
|
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