ENST00000255078.8:c.1848T>G
MANE Select
|
ENSP00000255078.4:p.Thr616=
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|
ENST00000674675.1:c.92T>G
|
|
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ENST00000674878.1:c.92T>G
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|
|
ENST00000674955.1:c.*565T>G
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ENSP00000502463.1:n.*565T>G
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|
ENST00000675118.1:c.1336T>G
|
|
|
ENST00000675389.1:n.123T>G
|
|
|
ENST00000675615.1:c.1848T>G
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ENSP00000502413.1:p.Thr616=
|
|
ENST00000675648.1:n.1223T>G
|
|
|
ENST00000675916.1:c.92T>G
|
|
|
ENST00000676173.1:n.2593T>G
|
|
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ENST00000676182.1:c.279T>G
|
|
|
ENST00000676228.1:c.*1171T>G
|
ENSP00000502375.1:n.*1171T>G
|
|
ENST00000255078.7:c.1848T>G
|
ENSP00000255078.3:p.Thr616=
|
|
ENST00000539064.5:n.1607T>G
|
|
|
ENST00000541229.5:n.543T>G
|
|
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ENST00000543739.5:n.841T>G
|
|
|
ENST00000545475.1:n.444T>G
|
|
|
NM_002180.2:c.1848T>G , LRG_250t1:c.1848T>G
|
NP_002171.2:p.Thr616=
|
|
XM_005273974.2:c.837T>G
|
XP_005274031.1:p.Thr279=
|
|
XM_005273975.2:c.720T>G
|
XP_005274032.1:p.Thr240=
|
|
XM_011544994.1:c.615T>G
|
XP_011543296.1:p.Thr205=
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XR_949903.1:n.1950T>G
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|
|
XM_005273975.3:c.720T>G
|
XP_005274032.1:p.Thr240=
|
|
XM_017017669.2:c.837T>G
|
XP_016873158.1:p.Thr279=
|
|
XM_017017670.2:c.837T>G
|
XP_016873159.1:p.Thr279=
|
|
XR_949903.3:n.1946T>G
|
|
|
NM_002180.3:c.1848T>G
MANE Select
|
NP_002171.2:p.Thr616=
|
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