ENST00000460843.6:c.2877T>G
MANE Select
|
ENSP00000417980.1:p.Leu959=
|
|
ENST00000636027.1:c.2763T>G
|
ENSP00000489961.1:p.Leu921=
|
|
ENST00000637161.1:c.2784T>G
|
ENSP00000490328.1:p.Leu928=
|
|
ENST00000637261.1:c.2917T>G
|
ENSP00000490815.1:n.2917T>G
|
|
ENST00000637891.1:c.771T>G
|
ENSP00000490907.1:p.Leu257=
|
|
ENST00000460843.5:c.2877T>G
|
ENSP00000417980.1:p.Leu959=
|
|
ENST00000462942.3:c.1734T>G
|
ENSP00000436107.1:p.Leu578=
|
|
ENST00000486164.5:c.564T>G
|
|
|
ENST00000488242.2:n.403T>G
|
|
|
NM_024757.4:c.2877T>G
|
NP_079033.4:p.Leu959=
|
|
XM_005266105.3:c.2868T>G
|
XP_005266162.1:p.Leu956=
|
|
XM_005266110.1:c.2784T>G
|
XP_005266167.1:p.Leu928=
|
|
XM_006717288.2:c.2859T>G
|
XP_006717351.1:p.Leu953=
|
|
XM_011519021.1:c.2886T>G
|
XP_011517323.1:p.Leu962=
|
|
XM_011519022.1:c.2883T>G
|
XP_011517324.1:p.Leu961=
|
|
XM_011519023.1:c.2865T>G
|
XP_011517325.1:p.Leu955=
|
|
XM_011519024.1:c.2808T>G
|
XP_011517326.1:p.Leu936=
|
|
XM_011519025.1:c.2784T>G
|
XP_011517327.1:p.Leu928=
|
|
XM_011519026.1:c.2742T>G
|
XP_011517328.1:p.Leu914=
|
|
XM_011519029.1:c.1308T>G
|
XP_011517331.1:p.Leu436=
|
|
XM_011519030.1:c.660T>G
|
XP_011517332.1:p.Leu220=
|
|
XM_011519031.1:c.447T>G
|
XP_011517333.1:p.Leu149=
|
|
XM_011519032.1:c.447T>G
|
XP_011517334.1:p.Leu149=
|
|
XM_011519033.1:c.2721T>G
|
XP_011517335.1:p.Leu907=
|
|
NM_001354263.1:c.2856T>G
|
NP_001341192.1:p.Leu952=
|
|
XM_005266105.5:c.2868T>G
|
XP_005266162.1:p.Leu956=
|
|
XM_011519021.3:c.2886T>G
|
XP_011517323.1:p.Leu962=
|
|
XM_011519022.3:c.2883T>G
|
XP_011517324.1:p.Leu961=
|
|
XM_011519023.3:c.2865T>G
|
XP_011517325.1:p.Leu955=
|
|
XM_011519029.3:c.1308T>G
|
XP_011517331.1:p.Leu436=
|
|
XM_011519030.3:c.660T>G
|
XP_011517332.1:p.Leu220=
|
|
XM_017015134.1:c.2862T>G
|
XP_016870623.1:p.Leu954=
|
|
XM_017015136.2:c.2778T>G
|
XP_016870625.1:p.Leu926=
|
|
XM_017015137.1:c.2763T>G
|
XP_016870626.1:p.Leu921=
|
|
XM_017015138.1:c.2763T>G
|
XP_016870627.1:p.Leu921=
|
|
XM_024447674.1:c.2706T>G
|
XP_024303442.1:p.Leu902=
|
|
XM_024447675.1:c.2640T>G
|
XP_024303443.1:p.Leu880=
|
|
XM_024447676.1:c.2001T>G
|
XP_024303444.1:p.Leu667=
|
|
XM_024447677.1:c.2001T>G
|
XP_024303445.1:p.Leu667=
|
|
XM_024447680.1:c.2619T>G
|
XP_024303448.1:p.Leu873=
|
|
NM_024757.5:c.2877T>G
MANE Select
|
NP_079033.4:p.Leu959=
|
|
NM_001354263.2:c.2856T>G
|
NP_001341192.1:p.Leu952=
|
|