ENST00000460843.6:c.2869C>T
MANE Select
|
ENSP00000417980.1:p.Leu957Phe
|
|
ENST00000636027.1:c.2755C>T
|
ENSP00000489961.1:p.Leu919Phe
|
|
ENST00000637161.1:c.2776C>T
|
ENSP00000490328.1:p.Leu926Phe
|
|
ENST00000637261.1:c.2909C>T
|
ENSP00000490815.1:n.2909C>T
|
|
ENST00000637891.1:c.763C>T
|
ENSP00000490907.1:p.Leu255Phe
|
|
ENST00000460843.5:c.2869C>T
|
ENSP00000417980.1:p.Leu957Phe
|
|
ENST00000462942.3:c.1726C>T
|
ENSP00000436107.1:p.Leu576Phe
|
|
ENST00000486164.5:c.556C>T
|
|
|
ENST00000488242.2:n.395C>T
|
|
|
NM_024757.4:c.2869C>T
|
NP_079033.4:p.Leu957Phe
|
|
XM_005266105.3:c.2860C>T
|
XP_005266162.1:p.Leu954Phe
|
|
XM_005266110.1:c.2776C>T
|
XP_005266167.1:p.Leu926Phe
|
|
XM_006717288.2:c.2851C>T
|
XP_006717351.1:p.Leu951Phe
|
|
XM_011519021.1:c.2878C>T
|
XP_011517323.1:p.Leu960Phe
|
|
XM_011519022.1:c.2875C>T
|
XP_011517324.1:p.Leu959Phe
|
|
XM_011519023.1:c.2857C>T
|
XP_011517325.1:p.Leu953Phe
|
|
XM_011519024.1:c.2800C>T
|
XP_011517326.1:p.Leu934Phe
|
|
XM_011519025.1:c.2776C>T
|
XP_011517327.1:p.Leu926Phe
|
|
XM_011519026.1:c.2734C>T
|
XP_011517328.1:p.Leu912Phe
|
|
XM_011519029.1:c.1300C>T
|
XP_011517331.1:p.Leu434Phe
|
|
XM_011519030.1:c.652C>T
|
XP_011517332.1:p.Leu218Phe
|
|
XM_011519031.1:c.439C>T
|
XP_011517333.1:p.Leu147Phe
|
|
XM_011519032.1:c.439C>T
|
XP_011517334.1:p.Leu147Phe
|
|
XM_011519033.1:c.2713C>T
|
XP_011517335.1:p.Leu905Phe
|
|
NM_001354263.1:c.2848C>T
|
NP_001341192.1:p.Leu950Phe
|
|
XM_005266105.5:c.2860C>T
|
XP_005266162.1:p.Leu954Phe
|
|
XM_011519021.3:c.2878C>T
|
XP_011517323.1:p.Leu960Phe
|
|
XM_011519022.3:c.2875C>T
|
XP_011517324.1:p.Leu959Phe
|
|
XM_011519023.3:c.2857C>T
|
XP_011517325.1:p.Leu953Phe
|
|
XM_011519029.3:c.1300C>T
|
XP_011517331.1:p.Leu434Phe
|
|
XM_011519030.3:c.652C>T
|
XP_011517332.1:p.Leu218Phe
|
|
XM_017015134.1:c.2854C>T
|
XP_016870623.1:p.Leu952Phe
|
|
XM_017015136.2:c.2770C>T
|
XP_016870625.1:p.Leu924Phe
|
|
XM_017015137.1:c.2755C>T
|
XP_016870626.1:p.Leu919Phe
|
|
XM_017015138.1:c.2755C>T
|
XP_016870627.1:p.Leu919Phe
|
|
XM_024447674.1:c.2698C>T
|
XP_024303442.1:p.Leu900Phe
|
|
XM_024447675.1:c.2632C>T
|
XP_024303443.1:p.Leu878Phe
|
|
XM_024447676.1:c.1993C>T
|
XP_024303444.1:p.Leu665Phe
|
|
XM_024447677.1:c.1993C>T
|
XP_024303445.1:p.Leu665Phe
|
|
XM_024447680.1:c.2611C>T
|
XP_024303448.1:p.Leu871Phe
|
|
NM_024757.5:c.2869C>T
MANE Select
|
NP_079033.4:p.Leu957Phe
|
|
NM_001354263.2:c.2848C>T
|
NP_001341192.1:p.Leu950Phe
|
|