ENST00000460843.6:c.2871C>T
MANE Select
|
ENSP00000417980.1:p.Leu957=
|
|
ENST00000636027.1:c.2757C>T
|
ENSP00000489961.1:p.Leu919=
|
|
ENST00000637161.1:c.2778C>T
|
ENSP00000490328.1:p.Leu926=
|
|
ENST00000637261.1:c.2911C>T
|
ENSP00000490815.1:n.2911C>T
|
|
ENST00000637891.1:c.765C>T
|
ENSP00000490907.1:p.Leu255=
|
|
ENST00000460843.5:c.2871C>T
|
ENSP00000417980.1:p.Leu957=
|
|
ENST00000462942.3:c.1728C>T
|
ENSP00000436107.1:p.Leu576=
|
|
ENST00000486164.5:c.558C>T
|
|
|
ENST00000488242.2:n.397C>T
|
|
|
NM_024757.4:c.2871C>T
|
NP_079033.4:p.Leu957=
|
|
XM_005266105.3:c.2862C>T
|
XP_005266162.1:p.Leu954=
|
|
XM_005266110.1:c.2778C>T
|
XP_005266167.1:p.Leu926=
|
|
XM_006717288.2:c.2853C>T
|
XP_006717351.1:p.Leu951=
|
|
XM_011519021.1:c.2880C>T
|
XP_011517323.1:p.Leu960=
|
|
XM_011519022.1:c.2877C>T
|
XP_011517324.1:p.Leu959=
|
|
XM_011519023.1:c.2859C>T
|
XP_011517325.1:p.Leu953=
|
|
XM_011519024.1:c.2802C>T
|
XP_011517326.1:p.Leu934=
|
|
XM_011519025.1:c.2778C>T
|
XP_011517327.1:p.Leu926=
|
|
XM_011519026.1:c.2736C>T
|
XP_011517328.1:p.Leu912=
|
|
XM_011519029.1:c.1302C>T
|
XP_011517331.1:p.Leu434=
|
|
XM_011519030.1:c.654C>T
|
XP_011517332.1:p.Leu218=
|
|
XM_011519031.1:c.441C>T
|
XP_011517333.1:p.Leu147=
|
|
XM_011519032.1:c.441C>T
|
XP_011517334.1:p.Leu147=
|
|
XM_011519033.1:c.2715C>T
|
XP_011517335.1:p.Leu905=
|
|
NM_001354263.1:c.2850C>T
|
NP_001341192.1:p.Leu950=
|
|
XM_005266105.5:c.2862C>T
|
XP_005266162.1:p.Leu954=
|
|
XM_011519021.3:c.2880C>T
|
XP_011517323.1:p.Leu960=
|
|
XM_011519022.3:c.2877C>T
|
XP_011517324.1:p.Leu959=
|
|
XM_011519023.3:c.2859C>T
|
XP_011517325.1:p.Leu953=
|
|
XM_011519029.3:c.1302C>T
|
XP_011517331.1:p.Leu434=
|
|
XM_011519030.3:c.654C>T
|
XP_011517332.1:p.Leu218=
|
|
XM_017015134.1:c.2856C>T
|
XP_016870623.1:p.Leu952=
|
|
XM_017015136.2:c.2772C>T
|
XP_016870625.1:p.Leu924=
|
|
XM_017015137.1:c.2757C>T
|
XP_016870626.1:p.Leu919=
|
|
XM_017015138.1:c.2757C>T
|
XP_016870627.1:p.Leu919=
|
|
XM_024447674.1:c.2700C>T
|
XP_024303442.1:p.Leu900=
|
|
XM_024447675.1:c.2634C>T
|
XP_024303443.1:p.Leu878=
|
|
XM_024447676.1:c.1995C>T
|
XP_024303444.1:p.Leu665=
|
|
XM_024447677.1:c.1995C>T
|
XP_024303445.1:p.Leu665=
|
|
XM_024447680.1:c.2613C>T
|
XP_024303448.1:p.Leu871=
|
|
NM_024757.5:c.2871C>T
MANE Select
|
NP_079033.4:p.Leu957=
|
|
NM_001354263.2:c.2850C>T
|
NP_001341192.1:p.Leu950=
|
|