ENST00000448723.2:c.2529+16T>C
MANE Select
|
ENSP00000391268.2:n.2529+16T>C
|
|
ENST00000368679.8:c.2538+16T>C
|
ENSP00000357668.4:n.2538+16T>C
|
|
NM_001288973.1:c.2529+16T>C
|
NP_001275902.1:n.2529+16T>C
|
|
NM_003474.5:c.2538+16T>C
|
NP_003465.3:n.2538+16T>C
|
|
XM_017016705.1:c.2070+16T>C
|
XP_016872194.1:n.2070+16T>C
|
|
XM_017016706.1:c.1371+16T>C
|
XP_016872195.1:n.1371+16T>C
|
|
XM_024448210.1:c.1200+16T>C
|
XP_024303978.1:n.1200+16T>C
|
|
NM_001288973.2:c.2529+16T>C
MANE Select
|
NP_001275902.1:n.2529+16T>C
|
|
NM_003474.6:c.2538+16T>C
|
NP_003465.3:n.2538+16T>C
|
|