ENST00000255078.8:c.2368C>G
MANE Select
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ENSP00000255078.4:p.Arg790Gly
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ENST00000674675.1:c.587+25C>G
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ENST00000674878.1:c.547+65C>G
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ENST00000674955.1:c.*1085C>G
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ENSP00000502463.1:n.*1085C>G
|
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ENST00000675118.1:c.1856C>G
|
|
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ENST00000675389.1:n.643C>G
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ENST00000675615.1:c.2368C>G
|
ENSP00000502413.1:p.Arg790Gly
|
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ENST00000675648.1:n.1743C>G
|
|
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ENST00000675916.1:c.612C>G
|
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ENST00000676173.1:n.3113C>G
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ENST00000676182.1:c.799C>G
|
|
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ENST00000676228.1:c.*1691C>G
|
ENSP00000502375.1:n.*1691C>G
|
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ENST00000255078.7:c.2368C>G
|
ENSP00000255078.3:p.Arg790Gly
|
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ENST00000539064.5:n.2127C>G
|
|
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ENST00000543739.5:n.1361C>G
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|
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NM_002180.2:c.2368C>G , LRG_250t1:c.2368C>G
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NP_002171.2:p.Arg790Gly
|
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XM_005273974.2:c.1357C>G
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XP_005274031.1:p.Arg453Gly
|
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XM_005273975.2:c.1240C>G
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XP_005274032.1:p.Arg414Gly
|
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XM_011544994.1:c.1135C>G
|
XP_011543296.1:p.Arg379Gly
|
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XR_949903.1:n.2470C>G
|
|
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XM_005273975.3:c.1240C>G
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XP_005274032.1:p.Arg414Gly
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XM_017017669.2:c.1357C>G
|
XP_016873158.1:p.Arg453Gly
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XM_017017670.2:c.1357C>G
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XP_016873159.1:p.Arg453Gly
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|
XR_949903.3:n.2466C>G
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|
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NM_002180.3:c.2368C>G
MANE Select
|
NP_002171.2:p.Arg790Gly
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