ENST00000265631.10:c.563T>C
MANE Select
|
ENSP00000265631.6:p.Val188Ala
|
|
ENST00000265631.9:c.563T>C
|
ENSP00000265631.5:p.Val188Ala
|
|
ENST00000416240.6:c.563T>C
|
ENSP00000400101.2:p.Val188Ala
|
|
NM_001160210.1:c.563T>C
|
NP_001153682.1:p.Val188Ala
|
|
NM_014251.2:c.563T>C
|
NP_055066.1:p.Val188Ala
|
|
NR_027662.1:n.638T>C
|
|
|
XM_006715831.2:c.596T>C
|
XP_006715894.1:p.Val199Ala
|
|
XM_011515727.1:c.596T>C
|
XP_011514029.1:p.Val199Ala
|
|
XM_006715831.4:c.596T>C
|
XP_006715894.1:p.Val199Ala
|
|
XM_011515727.3:c.596T>C
|
XP_011514029.1:p.Val199Ala
|
|
XM_017011663.1:c.554T>C
|
XP_016867152.1:p.Val185Ala
|
|
XM_017011664.2:c.-196T>C
|
XP_016867153.1:n.-196T>C
|
|
XM_017011665.1:c.-196T>C
|
XP_016867154.1:n.-196T>C
|
|
XR_001744525.2:n.734T>C
|
|
|
XR_002956405.1:n.876T>C
|
|
|
NM_014251.3:c.563T>C
MANE Select
|
NP_055066.1:p.Val188Ala
|
|
NR_027662.2:n.589T>C
|
|
|
NM_001160210.2:c.563T>C
|
NP_001153682.1:p.Val188Ala
|
|