ENST00000303941.4:c.2054T>C
MANE Select
|
ENSP00000306678.3:p.Val685Ala
|
|
ENST00000303941.3:c.2054T>C
|
ENSP00000306678.3:p.Val685Ala
|
|
NM_178510.1:c.2054T>C
|
NP_848605.1:p.Val685Ala
|
|
XM_011542736.1:c.2087T>C
|
XP_011541038.1:p.Val696Ala
|
|
XM_011542737.1:c.2057T>C
|
XP_011541039.1:p.Val686Ala
|
|
XM_011542738.1:c.1865T>C
|
XP_011541040.1:p.Val622Ala
|
|
XM_011542736.2:c.2087T>C
|
XP_011541038.1:p.Val696Ala
|
|
XM_011542737.2:c.2057T>C
|
XP_011541039.1:p.Val686Ala
|
|
XM_011542738.2:c.1865T>C
|
XP_011541040.1:p.Val622Ala
|
|
XM_017017475.1:c.2084T>C
|
XP_016872964.1:p.Val695Ala
|
|
NM_178510.2:c.2054T>C
MANE Select
|
NP_848605.1:p.Val685Ala
|
|