ENST00000243964.7:c.2991G>C
MANE Select
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ENSP00000243964.4:p.Gly997=
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ENST00000243964.6:c.2991G>C
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ENSP00000243964.3:p.Gly997=
|
|
ENST00000454036.6:c.3060G>C
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ENSP00000387694.1:p.Gly1020=
|
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ENST00000616201.4:c.1298-2211G>C
|
ENSP00000484585.1:n.1298-2211G>C
|
|
ENST00000616202.4:c.613-2036G>C
|
ENSP00000478369.1:n.613-2036G>C
|
|
ENST00000616933.4:c.*2309G>C
|
ENSP00000477569.1:n.*2309G>C
|
|
ENST00000626937.2:c.510-3154G>C
|
ENSP00000485953.1:n.510-3154G>C
|
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ENST00000628413.1:n.507G>C
|
|
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NM_001134771.1:c.3060G>C
|
NP_001128243.1:p.Gly1020=
|
|
NM_020708.4:c.2991G>C
|
NP_065759.1:p.Gly997=
|
|
XM_017027981.1:c.3060G>C
|
XP_016883470.1:p.Gly1020=
|
|
NM_001134771.2:c.3060G>C
|
NP_001128243.1:p.Gly1020=
|
|
NM_020708.5:c.2991G>C
MANE Select
|
NP_065759.1:p.Gly997=
|
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