ENST00000388798.7:c.939+190T>G
MANE Select
|
ENSP00000373450.3:n.939+190T>G
|
|
ENST00000251809.4:c.939+190T>G
|
ENSP00000251809.3:n.939+190T>G
|
|
ENST00000388798.6:c.939+190T>G
|
ENSP00000373450.2:n.939+190T>G
|
|
ENST00000520508.5:c.939+190T>G
|
ENSP00000428070.1:n.939+190T>G
|
|
ENST00000520643.5:c.939+190T>G
|
ENSP00000427716.1:n.939+190T>G
|
|
NM_003114.4:c.939+190T>G
|
NP_003105.2:n.939+190T>G
|
|
NM_172218.2:c.939+190T>G
|
NP_757367.1:n.939+190T>G
|
|
XM_011517240.1:c.939+190T>G
|
XP_011515542.1:n.939+190T>G
|
|
XM_011517241.1:c.939+190T>G
|
XP_011515543.1:n.939+190T>G
|
|
XM_011517242.1:c.939+190T>G
|
XP_011515544.1:n.939+190T>G
|
|
XM_011517243.1:c.939+190T>G
|
XP_011515545.1:n.939+190T>G
|
|
XM_011517244.1:c.939+190T>G
|
XP_011515546.1:n.939+190T>G
|
|
XM_011517245.1:c.939+190T>G
|
XP_011515547.1:n.939+190T>G
|
|
XM_011517240.2:c.939+190T>G
|
XP_011515542.1:n.939+190T>G
|
|
XM_011517241.2:c.939+190T>G
|
XP_011515543.1:n.939+190T>G
|
|
XM_011517242.2:c.939+190T>G
|
XP_011515544.1:n.939+190T>G
|
|
XM_011517243.2:c.939+190T>G
|
XP_011515545.1:n.939+190T>G
|
|
XM_011517245.2:c.939+190T>G
|
XP_011515547.1:n.939+190T>G
|
|
XM_017013754.1:c.1044+190T>G
|
XP_016869243.1:n.1044+190T>G
|
|
XM_017013755.1:c.603+190T>G
|
XP_016869244.1:n.603+190T>G
|
|
XR_001745580.1:n.1025+190T>G
|
|
|
XR_001745581.1:n.1025+190T>G
|
|
|
XR_001745582.1:n.1025+190T>G
|
|
|
XR_001745583.1:n.1025+190T>G
|
|
|
NM_001374321.1:c.939+190T>G
|
NP_001361250.1:n.939+190T>G
|
|
NM_003114.5:c.939+190T>G
MANE Select
|
NP_003105.2:n.939+190T>G
|
|
NM_172218.3:c.939+190T>G
|
NP_757367.1:n.939+190T>G
|
|