ENST00000318158.11:c.540T>C
MANE Select
|
ENSP00000313432.6:p.Phe180=
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|
ENST00000318158.10:c.540T>C
|
ENSP00000313432.6:p.Phe180=
|
|
ENST00000377824.8:n.577T>C
|
|
|
ENST00000460882.5:n.567T>C
|
|
|
ENST00000480596.5:n.1241T>C
|
|
|
ENST00000491488.5:n.245T>C
|
|
|
ENST00000494290.1:c.111T>C
|
ENSP00000432021.1:p.Phe37=
|
|
ENST00000497693.1:n.2073T>C
|
|
|
ENST00000607784.1:c.540T>C
|
ENSP00000475569.1:p.Phe180=
|
|
NM_012203.1:c.540T>C
|
NP_036335.1:p.Phe180=
|
|
XM_005251631.1:c.219T>C
|
XP_005251688.1:p.Phe73=
|
|
XM_011518073.1:c.138T>C
|
XP_011516375.1:p.Phe46=
|
|
XR_929374.1:n.985T>C
|
|
|
XM_017015320.2:c.540T>C
|
XP_016870809.1:p.Phe180=
|
|
XM_017015321.2:c.540T>C
|
XP_016870810.1:p.Phe180=
|
|
XM_017015323.2:c.138T>C
|
XP_016870812.1:p.Phe46=
|
|
XM_024447716.1:c.813T>C
|
XP_024303484.1:p.Phe271=
|
|
XM_024447717.1:c.813T>C
|
XP_024303485.1:p.Phe271=
|
|
XR_002956828.1:n.828T>C
|
|
|
XR_002956829.1:n.828T>C
|
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XR_002956830.1:n.599T>C
|
|
|
XR_002956831.1:n.274T>C
|
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|
XR_002956832.1:n.959T>C
|
|
|
NM_012203.2:c.540T>C
MANE Select
|
NP_036335.1:p.Phe180=
|
|