ENST00000286657.10:c.1614T>A
MANE Select
|
ENSP00000286657.4:p.Gly538=
|
|
ENST00000286657.8:c.1614T>A
|
ENSP00000286657.4:p.Gly538=
|
|
ENST00000622135.1:c.1614T>A
|
ENSP00000480055.1:p.Gly538=
|
|
NM_014243.2:c.1614T>A
|
NP_055058.2:p.Gly538=
|
|
XM_011532421.1:c.1557T>A
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XP_011530723.1:p.Gly519=
|
|
XM_011532422.1:c.1530T>A
|
XP_011530724.1:p.Gly510=
|
|
XM_011532423.1:c.972T>A
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XP_011530725.1:p.Gly324=
|
|
XM_011532424.1:c.882T>A
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XP_011530726.1:p.Gly294=
|
|
XM_011532421.2:c.1557T>A
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XP_011530723.1:p.Gly519=
|
|
XM_011532422.3:c.1530T>A
|
XP_011530724.1:p.Gly510=
|
|
NM_014243.3:c.1614T>A
MANE Select
|
NP_055058.2:p.Gly538=
|
|