ENST00000243964.7:c.3059G>T
MANE Select
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ENSP00000243964.4:p.Gly1020Val
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ENST00000243964.6:c.3059G>T
|
ENSP00000243964.3:p.Gly1020Val
|
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ENST00000454036.6:c.3128G>T
|
ENSP00000387694.1:p.Gly1043Val
|
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ENST00000616201.4:c.1298-2143G>T
|
ENSP00000484585.1:n.1298-2143G>T
|
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ENST00000616202.4:c.613-1968G>T
|
ENSP00000478369.1:n.613-1968G>T
|
|
ENST00000616933.4:c.*2377G>T
|
ENSP00000477569.1:n.*2377G>T
|
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ENST00000626937.2:c.510-3086G>T
|
ENSP00000485953.1:n.510-3086G>T
|
|
NM_001134771.1:c.3128G>T
|
NP_001128243.1:p.Gly1043Val
|
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NM_020708.4:c.3059G>T
|
NP_065759.1:p.Gly1020Val
|
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XM_017027981.1:c.3128G>T
|
XP_016883470.1:p.Gly1043Val
|
|
NM_001134771.2:c.3128G>T
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NP_001128243.1:p.Gly1043Val
|
|
NM_020708.5:c.3059G>T
MANE Select
|
NP_065759.1:p.Gly1020Val
|
|