ENST00000259455.4:c.1662+5122_1662+5123delinsGA
MANE Select
|
ENSP00000259455.2:n.1662+5122_1662+5123delinsGA
|
|
ENST00000637410.1:n.1440+5122_1440+5123delinsGA
|
|
|
ENST00000259455.3:c.1662+5122_1662+5123delinsGA
|
ENSP00000259455.2:n.1662+5122_1662+5123delinsGA
|
|
ENST00000634314.1:n.167+5122_167+5123delinsGA
|
|
|
NM_005458.7:c.1662+5122_1662+5123delinsGA
|
NP_005449.5:n.1662+5122_1662+5123delinsGA
|
|
XM_005252316.3:c.888+5122_888+5123delinsGA
|
XP_005252373.1:n.888+5122_888+5123delinsGA
|
|
XM_005252316.5:c.888+5122_888+5123delinsGA
|
XP_005252373.1:n.888+5122_888+5123delinsGA
|
|
XM_017015331.2:c.1368+5122_1368+5123delinsGA
|
XP_016870820.1:n.1368+5122_1368+5123delinsGA
|
|
XM_017015332.2:c.888+5122_888+5123delinsGA
|
XP_016870821.1:n.888+5122_888+5123delinsGA
|
|
NM_005458.8:c.1662+5122_1662+5123delinsGA
MANE Select
|
NP_005449.5:n.1662+5122_1662+5123delinsGA
|
|