ENST00000460843.6:c.2874T>G
MANE Select
|
ENSP00000417980.1:p.Phe958Leu
|
|
ENST00000636027.1:c.2760T>G
|
ENSP00000489961.1:p.Phe920Leu
|
|
ENST00000637161.1:c.2781T>G
|
ENSP00000490328.1:p.Phe927Leu
|
|
ENST00000637261.1:c.2914T>G
|
ENSP00000490815.1:n.2914T>G
|
|
ENST00000637891.1:c.768T>G
|
ENSP00000490907.1:p.Phe256Leu
|
|
ENST00000460843.5:c.2874T>G
|
ENSP00000417980.1:p.Phe958Leu
|
|
ENST00000462942.3:c.1731T>G
|
ENSP00000436107.1:p.Phe577Leu
|
|
ENST00000486164.5:c.561T>G
|
|
|
ENST00000488242.2:n.400T>G
|
|
|
NM_024757.4:c.2874T>G
|
NP_079033.4:p.Phe958Leu
|
|
XM_005266105.3:c.2865T>G
|
XP_005266162.1:p.Phe955Leu
|
|
XM_005266110.1:c.2781T>G
|
XP_005266167.1:p.Phe927Leu
|
|
XM_006717288.2:c.2856T>G
|
XP_006717351.1:p.Phe952Leu
|
|
XM_011519021.1:c.2883T>G
|
XP_011517323.1:p.Phe961Leu
|
|
XM_011519022.1:c.2880T>G
|
XP_011517324.1:p.Phe960Leu
|
|
XM_011519023.1:c.2862T>G
|
XP_011517325.1:p.Phe954Leu
|
|
XM_011519024.1:c.2805T>G
|
XP_011517326.1:p.Phe935Leu
|
|
XM_011519025.1:c.2781T>G
|
XP_011517327.1:p.Phe927Leu
|
|
XM_011519026.1:c.2739T>G
|
XP_011517328.1:p.Phe913Leu
|
|
XM_011519029.1:c.1305T>G
|
XP_011517331.1:p.Phe435Leu
|
|
XM_011519030.1:c.657T>G
|
XP_011517332.1:p.Phe219Leu
|
|
XM_011519031.1:c.444T>G
|
XP_011517333.1:p.Phe148Leu
|
|
XM_011519032.1:c.444T>G
|
XP_011517334.1:p.Phe148Leu
|
|
XM_011519033.1:c.2718T>G
|
XP_011517335.1:p.Phe906Leu
|
|
NM_001354263.1:c.2853T>G
|
NP_001341192.1:p.Phe951Leu
|
|
XM_005266105.5:c.2865T>G
|
XP_005266162.1:p.Phe955Leu
|
|
XM_011519021.3:c.2883T>G
|
XP_011517323.1:p.Phe961Leu
|
|
XM_011519022.3:c.2880T>G
|
XP_011517324.1:p.Phe960Leu
|
|
XM_011519023.3:c.2862T>G
|
XP_011517325.1:p.Phe954Leu
|
|
XM_011519029.3:c.1305T>G
|
XP_011517331.1:p.Phe435Leu
|
|
XM_011519030.3:c.657T>G
|
XP_011517332.1:p.Phe219Leu
|
|
XM_017015134.1:c.2859T>G
|
XP_016870623.1:p.Phe953Leu
|
|
XM_017015136.2:c.2775T>G
|
XP_016870625.1:p.Phe925Leu
|
|
XM_017015137.1:c.2760T>G
|
XP_016870626.1:p.Phe920Leu
|
|
XM_017015138.1:c.2760T>G
|
XP_016870627.1:p.Phe920Leu
|
|
XM_024447674.1:c.2703T>G
|
XP_024303442.1:p.Phe901Leu
|
|
XM_024447675.1:c.2637T>G
|
XP_024303443.1:p.Phe879Leu
|
|
XM_024447676.1:c.1998T>G
|
XP_024303444.1:p.Phe666Leu
|
|
XM_024447677.1:c.1998T>G
|
XP_024303445.1:p.Phe666Leu
|
|
XM_024447680.1:c.2616T>G
|
XP_024303448.1:p.Phe872Leu
|
|
NM_024757.5:c.2874T>G
MANE Select
|
NP_079033.4:p.Phe958Leu
|
|
NM_001354263.2:c.2853T>G
|
NP_001341192.1:p.Phe951Leu
|
|