ENST00000375708.4:c.2552T>G
MANE Select
|
ENSP00000364860.3:p.Val851Gly
|
|
ENST00000375708.3:c.2552T>G
|
ENSP00000364860.3:p.Val851Gly
|
|
ENST00000375715.5:c.1920+212T>G
|
ENSP00000364867.1:n.1920+212T>G
|
|
ENST00000550066.5:n.3020T>G
|
|
|
NM_004560.3:c.2552T>G
|
NP_004551.2:p.Val851Gly
|
|
XM_005252008.3:c.2132T>G
|
XP_005252065.1:p.Val711Gly
|
|
XM_005252009.3:c.1349T>G
|
XP_005252066.1:p.Val450Gly
|
|
XM_006717121.2:c.2132T>G
|
XP_006717184.1:p.Val711Gly
|
|
XM_011518721.1:c.2132T>G
|
XP_011517023.1:p.Val711Gly
|
|
XM_005252008.4:c.2132T>G
|
XP_005252065.1:p.Val711Gly
|
|
XM_006717121.3:c.2132T>G
|
XP_006717184.1:p.Val711Gly
|
|
XM_017014762.1:c.2543T>G
|
XP_016870251.1:p.Val848Gly
|
|
XM_017014763.1:c.2132T>G
|
XP_016870252.1:p.Val711Gly
|
|
NM_004560.4:c.2552T>G
MANE Select
|
NP_004551.2:p.Val851Gly
|
|