ENST00000241453.12:c.1736T>G
MANE Select
|
ENSP00000241453.7:p.Val579Gly
|
|
ENST00000241453.11:c.1736T>G
|
ENSP00000241453.7:p.Val579Gly
|
|
ENST00000380987.2:c.1736T>G
|
ENSP00000370374.2:p.Val579Gly
|
|
NM_004119.2:c.1736T>G , LRG_457t1:c.1736T>G
|
NP_004110.2:p.Val579Gly
|
|
NR_130706.1:n.1818T>G
|
|
|
XM_011535015.1:c.1679T>G
|
XP_011533317.1:p.Val560Gly
|
|
XM_011535016.1:c.1211T>G
|
XP_011533318.1:p.Val404Gly
|
|
XM_011535017.1:c.1211T>G
|
XP_011533319.1:p.Val404Gly
|
|
XM_011535018.1:c.1211T>G
|
XP_011533320.1:p.Val404Gly
|
|
XM_011535015.2:c.1679T>G
|
XP_011533317.1:p.Val560Gly
|
|
XM_011535017.2:c.1211T>G
|
XP_011533319.1:p.Val404Gly
|
|
XM_011535018.2:c.1211T>G
|
XP_011533320.1:p.Val404Gly
|
|
XM_017020486.1:c.1520T>G
|
XP_016875975.1:p.Val507Gly
|
|
XM_017020487.1:c.1211T>G
|
XP_016875976.1:p.Val404Gly
|
|
XM_017020488.1:c.857T>G
|
XP_016875977.1:p.Val286Gly
|
|
XM_017020489.1:c.839T>G
|
XP_016875978.1:p.Val280Gly
|
|
NM_004119.3:c.1736T>G
MANE Select
|
NP_004110.2:p.Val579Gly
|
|
NR_130706.2:n.1802T>G
|
|
|