ENST00000460843.6:c.2875C>A
MANE Select
|
ENSP00000417980.1:p.Leu959Ile
|
|
ENST00000636027.1:c.2761C>A
|
ENSP00000489961.1:p.Leu921Ile
|
|
ENST00000637161.1:c.2782C>A
|
ENSP00000490328.1:p.Leu928Ile
|
|
ENST00000637261.1:c.2915C>A
|
ENSP00000490815.1:n.2915C>A
|
|
ENST00000637891.1:c.769C>A
|
ENSP00000490907.1:p.Leu257Ile
|
|
ENST00000460843.5:c.2875C>A
|
ENSP00000417980.1:p.Leu959Ile
|
|
ENST00000462942.3:c.1732C>A
|
ENSP00000436107.1:p.Leu578Ile
|
|
ENST00000486164.5:c.562C>A
|
|
|
ENST00000488242.2:n.401C>A
|
|
|
NM_024757.4:c.2875C>A
|
NP_079033.4:p.Leu959Ile
|
|
XM_005266105.3:c.2866C>A
|
XP_005266162.1:p.Leu956Ile
|
|
XM_005266110.1:c.2782C>A
|
XP_005266167.1:p.Leu928Ile
|
|
XM_006717288.2:c.2857C>A
|
XP_006717351.1:p.Leu953Ile
|
|
XM_011519021.1:c.2884C>A
|
XP_011517323.1:p.Leu962Ile
|
|
XM_011519022.1:c.2881C>A
|
XP_011517324.1:p.Leu961Ile
|
|
XM_011519023.1:c.2863C>A
|
XP_011517325.1:p.Leu955Ile
|
|
XM_011519024.1:c.2806C>A
|
XP_011517326.1:p.Leu936Ile
|
|
XM_011519025.1:c.2782C>A
|
XP_011517327.1:p.Leu928Ile
|
|
XM_011519026.1:c.2740C>A
|
XP_011517328.1:p.Leu914Ile
|
|
XM_011519029.1:c.1306C>A
|
XP_011517331.1:p.Leu436Ile
|
|
XM_011519030.1:c.658C>A
|
XP_011517332.1:p.Leu220Ile
|
|
XM_011519031.1:c.445C>A
|
XP_011517333.1:p.Leu149Ile
|
|
XM_011519032.1:c.445C>A
|
XP_011517334.1:p.Leu149Ile
|
|
XM_011519033.1:c.2719C>A
|
XP_011517335.1:p.Leu907Ile
|
|
NM_001354263.1:c.2854C>A
|
NP_001341192.1:p.Leu952Ile
|
|
XM_005266105.5:c.2866C>A
|
XP_005266162.1:p.Leu956Ile
|
|
XM_011519021.3:c.2884C>A
|
XP_011517323.1:p.Leu962Ile
|
|
XM_011519022.3:c.2881C>A
|
XP_011517324.1:p.Leu961Ile
|
|
XM_011519023.3:c.2863C>A
|
XP_011517325.1:p.Leu955Ile
|
|
XM_011519029.3:c.1306C>A
|
XP_011517331.1:p.Leu436Ile
|
|
XM_011519030.3:c.658C>A
|
XP_011517332.1:p.Leu220Ile
|
|
XM_017015134.1:c.2860C>A
|
XP_016870623.1:p.Leu954Ile
|
|
XM_017015136.2:c.2776C>A
|
XP_016870625.1:p.Leu926Ile
|
|
XM_017015137.1:c.2761C>A
|
XP_016870626.1:p.Leu921Ile
|
|
XM_017015138.1:c.2761C>A
|
XP_016870627.1:p.Leu921Ile
|
|
XM_024447674.1:c.2704C>A
|
XP_024303442.1:p.Leu902Ile
|
|
XM_024447675.1:c.2638C>A
|
XP_024303443.1:p.Leu880Ile
|
|
XM_024447676.1:c.1999C>A
|
XP_024303444.1:p.Leu667Ile
|
|
XM_024447677.1:c.1999C>A
|
XP_024303445.1:p.Leu667Ile
|
|
XM_024447680.1:c.2617C>A
|
XP_024303448.1:p.Leu873Ile
|
|
NM_024757.5:c.2875C>A
MANE Select
|
NP_079033.4:p.Leu959Ile
|
|
NM_001354263.2:c.2854C>A
|
NP_001341192.1:p.Leu952Ile
|
|