ENST00000318158.11:c.930T=
MANE Select
|
ENSP00000313432.6:p.Ala310=
|
|
ENST00000318158.10:c.930T=
|
ENSP00000313432.6:p.Ala310=
|
|
ENST00000460882.5:n.957T=
|
|
|
ENST00000480596.5:n.1631T=
|
|
|
ENST00000494290.1:c.*52-156T=
|
ENSP00000432021.1:n.*52-156T=
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|
ENST00000497693.1:n.4498T=
|
|
|
NM_012203.1:c.930T=
|
NP_036335.1:p.Ala310=
|
|
XM_005251631.1:c.609T=
|
XP_005251688.1:p.Ala203=
|
|
XM_011518073.1:c.528T=
|
XP_011516375.1:p.Ala176=
|
|
XM_017015320.2:c.946-686T=
|
XP_016870809.1:n.946-686T=
|
|
XM_017015321.2:c.866-686T=
|
XP_016870810.1:n.866-686T=
|
|
XM_017015323.2:c.544-686T=
|
XP_016870812.1:n.544-686T=
|
|
XM_024447716.1:c.1219-686T=
|
XP_024303484.1:n.1219-686T=
|
|
XM_024447717.1:c.1139-686T=
|
XP_024303485.1:n.1139-686T=
|
|
XR_002956828.1:n.1234-686T=
|
|
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XR_002956829.1:n.1154-686T=
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|
|
XR_002956830.1:n.2350T=
|
|
|
XR_002956831.1:n.2025T=
|
|
|
XR_002956832.1:n.1349T=
|
|
|
NM_012203.2:c.930T=
MANE Select
|
NP_036335.1:p.Ala310=
|
|