ENST00000265631.10:c.1909G>T
MANE Select
|
ENSP00000265631.6:p.Val637Phe
|
|
ENST00000265631.9:c.1909G>T
|
ENSP00000265631.5:p.Val637Phe
|
|
ENST00000416240.6:c.1912G>T
|
ENSP00000400101.2:p.Val638Phe
|
|
ENST00000494085.1:n.412G>T
|
|
|
NM_001160210.1:c.1912G>T
|
NP_001153682.1:p.Val638Phe
|
|
NM_014251.2:c.1909G>T
|
NP_055066.1:p.Val637Phe
|
|
NR_027662.1:n.1984G>T
|
|
|
XM_006715831.2:c.1942G>T
|
XP_006715894.1:p.Val648Phe
|
|
XM_011515728.1:c.1057G>T
|
XP_011514030.1:p.Val353Phe
|
|
XM_006715831.4:c.1942G>T
|
XP_006715894.1:p.Val648Phe
|
|
XM_017011663.1:c.1900G>T
|
XP_016867152.1:p.Val634Phe
|
|
XM_017011664.2:c.1057G>T
|
XP_016867153.1:p.Val353Phe
|
|
XM_017011665.1:c.1057G>T
|
XP_016867154.1:p.Val353Phe
|
|
XR_001744525.2:n.2155G>T
|
|
|
XR_002956405.1:n.2713G>T
|
|
|
NM_014251.3:c.1909G>T
MANE Select
|
NP_055066.1:p.Val637Phe
|
|
NR_027662.2:n.1935G>T
|
|
|
NM_001160210.2:c.1912G>T
|
NP_001153682.1:p.Val638Phe
|
|