ENST00000497571.6:c.552T>A
MANE Select
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ENSP00000419923.1:p.Gly184=
|
|
ENST00000173785.4:n.257+30T>A
|
|
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ENST00000469435.1:c.552T>A
|
ENSP00000419079.1:p.Gly184=
|
|
ENST00000497571.5:c.552T>A
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ENSP00000419923.1:p.Gly184=
|
|
ENST00000542957.1:c.552T>A
|
ENSP00000445301.1:p.Gly184=
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|
NM_001160124.1:c.550+2T>A
|
NP_001153596.1:n.550+2T>A
|
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NM_001160125.1:c.552T>A
|
NP_001153597.1:p.Gly184=
|
|
NM_001300.5:c.552T>A
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NP_001291.3:p.Gly184=
|
|
NR_027653.1:n.789+30T>A
|
|
|
NM_001300.6:c.552T>A
MANE Select
|
NP_001291.3:p.Gly184=
|
|
NM_001160124.2:c.550+2T>A
|
NP_001153596.1:n.550+2T>A
|
|
NR_027653.2:n.717+30T>A
|
|
|
NM_001160125.2:c.552T>A
|
NP_001153597.1:p.Gly184=
|
|