ENST00000631182.3:c.4777G>T
MANE Plus Clinical
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ENSP00000486885.1:p.Gly1593Ter
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ENST00000375437.7:c.4777G>T
MANE Select
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ENSP00000364586.2:p.Gly1593Ter
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ENST00000636071.2:c.4777G>T
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ENSP00000490107.1:p.Gly1593Ter
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ENST00000636135.1:c.*3096G>T
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ENSP00000489821.1:n.*3096G>T
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ENST00000636384.2:c.*2764G>T
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ENSP00000490765.1:n.*2764G>T
|
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ENST00000636662.2:c.*5300G>T
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ENSP00000489873.1:n.*5300G>T
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ENST00000636769.1:c.*2719G>T
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ENSP00000490800.1:n.*2719G>T
|
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ENST00000636985.2:c.4381G>T
|
ENSP00000490849.1:p.Gly1461Ter
|
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ENST00000637266.2:c.4777G>T
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ENSP00000490866.1:p.Gly1593Ter
|
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ENST00000283256.10:c.4777G>T
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ENSP00000283256.6:p.Gly1593Ter
|
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ENST00000375427.4:c.4777G>T
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ENSP00000364576.2:p.Gly1593Ter
|
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ENST00000375437.6:c.4777G>T
|
ENSP00000364586.2:p.Gly1593Ter
|
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ENST00000480032.4:n.8208G>T
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|
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ENST00000631182.2:c.4777G>T
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ENSP00000486885.1:p.Gly1593Ter
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NM_001040142.1:c.4777G>T
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NP_001035232.1:p.Gly1593Ter
|
|
NM_001040143.1:c.4777G>T
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NP_001035233.1:p.Gly1593Ter
|
|
NM_021007.2:c.4777G>T
|
NP_066287.2:p.Gly1593Ter
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XM_005246750.2:c.4777G>T
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XP_005246807.1:p.Gly1593Ter
|
|
XM_005246753.2:c.4777G>T
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XP_005246810.1:p.Gly1593Ter
|
|
XM_005246754.3:c.4747G>T
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XP_005246811.1:p.Gly1583Ter
|
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XM_005246755.3:c.4024G>T
|
XP_005246812.1:p.Gly1342Ter
|
|
XM_011511608.1:c.4777G>T
|
XP_011509910.1:p.Gly1593Ter
|
|
XM_011511609.1:c.4777G>T
|
XP_011509911.1:p.Gly1593Ter
|
|
XM_005246753.3:c.4777G>T
|
XP_005246810.1:p.Gly1593Ter
|
|
XM_017004656.1:c.4777G>T
|
XP_016860145.1:p.Gly1593Ter
|
|
XM_017004657.1:c.4777G>T
|
XP_016860146.1:p.Gly1593Ter
|
|
XM_017004658.1:c.4024G>T
|
XP_016860147.1:p.Gly1342Ter
|
|
XM_017004659.1:c.2575G>T
|
XP_016860148.1:p.Gly859Ter
|
|
XM_024453037.1:c.4024G>T
|
XP_024308805.1:p.Gly1342Ter
|
|
NM_001040142.2:c.4777G>T
MANE Select
|
NP_001035232.1:p.Gly1593Ter
|
|
NM_001040143.2:c.4777G>T
|
NP_001035233.1:p.Gly1593Ter
|
|
NM_001371246.1:c.4777G>T
MANE Plus Clinical
|
NP_001358175.1:p.Gly1593Ter
|
|
NM_001371247.1:c.4777G>T
|
NP_001358176.1:p.Gly1593Ter
|
|
NM_021007.3:c.4777G>T
|
NP_066287.2:p.Gly1593Ter
|
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