ENST00000302068.9:c.1174G=
MANE Select
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ENSP00000306099.4:p.Gly392=
|
|
ENST00000302068.8:c.1174G=
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ENSP00000306099.4:p.Gly392=
|
|
ENST00000502545.5:n.939+422G=
|
|
|
ENST00000509493.1:c.517G=
|
ENSP00000426757.1:p.Gly173=
|
|
NM_001184741.1:c.997G=
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NP_001171670.1:p.Gly333=
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|
NM_005141.4:c.1174G= , LRG_558t1:c.1174G=
|
NP_005132.2:p.Gly392=
|
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NM_001382759.1:c.1042G=
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NP_001369688.1:p.Gly348=
|
|
NM_001382760.1:c.1174G=
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NP_001369689.1:p.Gly392=
|
|
NM_001382761.1:c.1174G=
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NP_001369690.1:p.Gly392=
|
|
NM_001382762.1:c.874G=
|
NP_001369691.1:p.Gly292=
|
|
NM_001382763.1:c.1165G=
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NP_001369692.1:p.Gly389=
|
|
NM_001382764.1:c.1081-44G=
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NP_001369693.1:n.1081-44G=
|
|
NM_001382765.1:c.1174G=
|
NP_001369694.1:p.Gly392=
|
|
NM_005141.5:c.1174G=
MANE Select
|
NP_005132.2:p.Gly392=
|
|