ENST00000460843.6:c.3125C>T
MANE Select
|
ENSP00000417980.1:p.Ser1042Phe
|
|
ENST00000637161.1:c.3032C>T
|
ENSP00000490328.1:p.Ser1011Phe
|
|
ENST00000637261.1:c.3165C>T
|
ENSP00000490815.1:n.3165C>T
|
|
ENST00000637891.1:c.1019C>T
|
ENSP00000490907.1:p.Ser340Phe
|
|
ENST00000460843.5:c.3125C>T
|
ENSP00000417980.1:p.Ser1042Phe
|
|
ENST00000462942.3:c.1982C>T
|
ENSP00000436107.1:p.Ser661Phe
|
|
ENST00000488242.2:n.651C>T
|
|
|
NM_024757.4:c.3125C>T
|
NP_079033.4:p.Ser1042Phe
|
|
XM_005266105.3:c.3116C>T
|
XP_005266162.1:p.Ser1039Phe
|
|
XM_005266110.1:c.3032C>T
|
XP_005266167.1:p.Ser1011Phe
|
|
XM_006717288.2:c.3107C>T
|
XP_006717351.1:p.Ser1036Phe
|
|
XM_011519021.1:c.3134C>T
|
XP_011517323.1:p.Ser1045Phe
|
|
XM_011519022.1:c.3131C>T
|
XP_011517324.1:p.Ser1044Phe
|
|
XM_011519023.1:c.3113C>T
|
XP_011517325.1:p.Ser1038Phe
|
|
XM_011519024.1:c.3056C>T
|
XP_011517326.1:p.Ser1019Phe
|
|
XM_011519025.1:c.3032C>T
|
XP_011517327.1:p.Ser1011Phe
|
|
XM_011519026.1:c.2990C>T
|
XP_011517328.1:p.Ser997Phe
|
|
XM_011519029.1:c.1556C>T
|
XP_011517331.1:p.Ser519Phe
|
|
XM_011519030.1:c.908C>T
|
XP_011517332.1:p.Ser303Phe
|
|
XM_011519031.1:c.695C>T
|
XP_011517333.1:p.Ser232Phe
|
|
XM_011519032.1:c.695C>T
|
XP_011517334.1:p.Ser232Phe
|
|
XM_011519033.1:c.2969C>T
|
XP_011517335.1:p.Ser990Phe
|
|
NM_001354263.1:c.3104C>T
|
NP_001341192.1:p.Ser1035Phe
|
|
XM_005266105.5:c.3116C>T
|
XP_005266162.1:p.Ser1039Phe
|
|
XM_011519021.3:c.3134C>T
|
XP_011517323.1:p.Ser1045Phe
|
|
XM_011519022.3:c.3131C>T
|
XP_011517324.1:p.Ser1044Phe
|
|
XM_011519023.3:c.3113C>T
|
XP_011517325.1:p.Ser1038Phe
|
|
XM_011519029.3:c.1556C>T
|
XP_011517331.1:p.Ser519Phe
|
|
XM_011519030.3:c.908C>T
|
XP_011517332.1:p.Ser303Phe
|
|
XM_017015134.1:c.3110C>T
|
XP_016870623.1:p.Ser1037Phe
|
|
XM_017015136.2:c.3026C>T
|
XP_016870625.1:p.Ser1009Phe
|
|
XM_017015137.1:c.3011C>T
|
XP_016870626.1:p.Ser1004Phe
|
|
XM_017015138.1:c.3011C>T
|
XP_016870627.1:p.Ser1004Phe
|
|
XM_024447674.1:c.2954C>T
|
XP_024303442.1:p.Ser985Phe
|
|
XM_024447675.1:c.2888C>T
|
XP_024303443.1:p.Ser963Phe
|
|
XM_024447676.1:c.2249C>T
|
XP_024303444.1:p.Ser750Phe
|
|
XM_024447677.1:c.2249C>T
|
XP_024303445.1:p.Ser750Phe
|
|
XM_024447680.1:c.2867C>T
|
XP_024303448.1:p.Ser956Phe
|
|
NM_024757.5:c.3125C>T
MANE Select
|
NP_079033.4:p.Ser1042Phe
|
|
NM_001354263.2:c.3104C>T
|
NP_001341192.1:p.Ser1035Phe
|
|