ENST00000337138.9:c.1766G>C
(HIF1A)
MANE Select
|
ENSP00000338018.4:p.Ser589Thr
|
|
ENST00000323441.10:c.1766G>C
(HIF1A)
|
ENSP00000323326.6:p.Ser589Thr
|
|
ENST00000337138.8:c.1766G>C
(HIF1A)
|
ENSP00000338018.4:p.Ser589Thr
|
|
ENST00000394997.5:c.1769G>C
(HIF1A)
|
ENSP00000378446.1:p.Ser590Thr
|
|
ENST00000539097.2:c.1838G>C
(HIF1A)
|
ENSP00000437955.1:p.Ser613Thr
|
|
ENST00000547430.2:n.674G>C
(HIF1A)
|
|
|
ENST00000555014.1:n.412G>C
(HIF1A)
|
|
|
ENST00000557538.5:c.1589G>C
(HIF1A)
|
ENSP00000451696.1:p.Ser530Thr
|
|
NM_001243084.1:c.1838G>C
(HIF1A)
|
NP_001230013.1:p.Ser613Thr
|
|
NM_001530.3:c.1766G>C
(HIF1A)
|
NP_001521.1:p.Ser589Thr
|
|
NM_181054.2:c.1766G>C
(HIF1A)
|
NP_851397.1:p.Ser589Thr
|
|
XR_943925.1:n.213+10024C>G
(HIF1A-AS3)
|
|
|
XR_943926.1:n.213+10024C>G
(HIF1A-AS3)
|
|
|
XR_943927.1:n.213+10024C>G
(HIF1A-AS3)
|
|
|
XR_943928.1:n.213+10024C>G
(HIF1A-AS3)
|
|
|
XR_943929.1:n.213+10024C>G
(HIF1A-AS3)
|
|
|
NR_144368.1:n.213+10024C>G
(HIF1A-AS3)
|
|
|
NM_001530.4:c.1766G>C
(HIF1A)
MANE Select
|
NP_001521.1:p.Ser589Thr
|
|
NM_181054.3:c.1766G>C
(HIF1A)
|
NP_851397.1:p.Ser589Thr
|
|
NM_001243084.2:c.1838G>C
(HIF1A)
|
NP_001230013.1:p.Ser613Thr
|
|