ENST00000318158.11:c.987G>C
MANE Select
|
ENSP00000313432.6:p.Ter329Tyr
|
|
ENST00000318158.10:c.987G>C
|
ENSP00000313432.6:p.Ter329Tyr
|
|
ENST00000460882.5:n.1014G>C
|
|
|
ENST00000480596.5:n.1688G>C
|
|
|
ENST00000494290.1:c.*52-99G>C
|
ENSP00000432021.1:n.*52-99G>C
|
|
ENST00000497693.1:n.4555G>C
|
|
|
NM_012203.1:c.987G>C
|
NP_036335.1:p.Ter329Tyr
|
|
XM_005251631.1:c.666G>C
|
XP_005251688.1:p.Ter222Tyr
|
|
XM_011518073.1:c.585G>C
|
XP_011516375.1:p.Ter195Tyr
|
|
XM_017015320.2:c.946-629G>C
|
XP_016870809.1:n.946-629G>C
|
|
XM_017015321.2:c.866-629G>C
|
XP_016870810.1:n.866-629G>C
|
|
XM_017015323.2:c.544-629G>C
|
XP_016870812.1:n.544-629G>C
|
|
XM_024447716.1:c.1219-629G>C
|
XP_024303484.1:n.1219-629G>C
|
|
XM_024447717.1:c.1139-629G>C
|
XP_024303485.1:n.1139-629G>C
|
|
XR_002956828.1:n.1234-629G>C
|
|
|
XR_002956829.1:n.1154-629G>C
|
|
|
XR_002956830.1:n.2407G>C
|
|
|
XR_002956831.1:n.2082G>C
|
|
|
XR_002956832.1:n.1406G>C
|
|
|
NM_012203.2:c.987G>C
MANE Select
|
NP_036335.1:p.Ter329Tyr
|
|