ENST00000389857.11:c.5068A>G
MANE Select
|
ENSP00000374507.6:p.Ser1690Gly
|
|
ENST00000331194.8:c.640A>G
|
ENSP00000330332.8:p.Ser214Gly
|
|
ENST00000334448.5:n.880A>G
|
|
|
ENST00000389857.10:c.5068A>G
|
ENSP00000374507.6:p.Ser1690Gly
|
|
ENST00000556726.5:c.1296A>G
|
|
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NM_001080414.3:c.5068A>G
|
NP_001073883.2:p.Ser1690Gly
|
|
XM_011536796.1:c.4960A>G
|
XP_011535098.1:p.Ser1654Gly
|
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XR_429316.2:n.5343A>G
|
|
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XM_011536796.2:c.4960A>G
|
XP_011535098.1:p.Ser1654Gly
|
|
XM_017021336.1:c.2149A>G
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XP_016876825.1:p.Ser717Gly
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XR_429316.4:n.5341A>G
|
|
|
NM_001080414.4:c.5068A>G
MANE Select
|
NP_001073883.2:p.Ser1690Gly
|
|