ENST00000265631.10:c.860T>G
MANE Select
|
ENSP00000265631.6:p.Leu287Ter
|
|
ENST00000265631.9:c.860T>G
|
ENSP00000265631.5:p.Leu287Ter
|
|
ENST00000416240.6:c.860T>G
|
ENSP00000400101.2:p.Leu287Ter
|
|
ENST00000484495.5:n.13T>G
|
|
|
NM_001160210.1:c.860T>G
|
NP_001153682.1:p.Leu287Ter
|
|
NM_014251.2:c.860T>G
|
NP_055066.1:p.Leu287Ter
|
|
NR_027662.1:n.935T>G
|
|
|
XM_006715831.2:c.893T>G
|
XP_006715894.1:p.Leu298Ter
|
|
XM_011515727.1:c.893T>G
|
XP_011514029.1:p.Leu298Ter
|
|
XM_011515728.1:c.8T>G
|
XP_011514030.1:p.Leu3Ter
|
|
XM_006715831.4:c.893T>G
|
XP_006715894.1:p.Leu298Ter
|
|
XM_011515727.3:c.893T>G
|
XP_011514029.1:p.Leu298Ter
|
|
XM_017011663.1:c.851T>G
|
XP_016867152.1:p.Leu284Ter
|
|
XM_017011664.2:c.8T>G
|
XP_016867153.1:p.Leu3Ter
|
|
XM_017011665.1:c.8T>G
|
XP_016867154.1:p.Leu3Ter
|
|
XR_001744525.2:n.1031T>G
|
|
|
XR_002956405.1:n.1173T>G
|
|
|
NM_014251.3:c.860T>G
MANE Select
|
NP_055066.1:p.Leu287Ter
|
|
NR_027662.2:n.886T>G
|
|
|
NM_001160210.2:c.860T>G
|
NP_001153682.1:p.Leu287Ter
|
|